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(2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate

    Specifications

    HS Code

    139491

    Chemical Name (2R,3S)-2-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl)morpholine 4-methylbenzenesulfonate
    Molecular Formula C31H29F7NO5S
    Molecular Weight 663.62 g/mol
    Appearance Solid (usually)
    Solubility Solubility characteristics depend on solvent (e.g., likely sparingly soluble in water, more soluble in organic solvents like dichloromethane, DMSO)
    Melting Point Specific melting point data would require experimental determination
    Boiling Point Boiling point would be difficult to directly define as may decompose before boiling, and is highly solvent - dependent
    Pka No common pKa data found without experimental determination, acidic - basic properties depend on functional groups
    Logp Estimated logP would suggest lipophilic nature due to fluorinated and aromatic groups
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

    As an accredited (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of [(2R,3S)-2-((R)-1-(3,5 - Bis(trifluoromethyl)phenyl)ethoxy)-3-(4 - fluorophenyl)morpholine 4 - Methylbenzenesulfonate] packaged in sealed bags.
    Storage (2R,3S)-2-((R)-1-(3,5 - Bis(trifluoromethyl)phenyl)ethoxy)-3-(4 - fluorophenyl)morpholine 4 - methylbenzenesulfonate should be stored in a cool, dry place, away from direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and exposure to air, as these conditions could potentially degrade the chemical. Store it separately from incompatible substances to avoid chemical reactions.
    Shipping The shipping of (2R,3S)-2-[(R)-1-(3,5 - Bis(trifluoromethyl)phenyl)ethoxy]-3-(4 - fluorophenyl) morpholine 4 - methylbenzenesulfonate must adhere to strict regulations for chemicals. It should be properly packaged to prevent damage and spills during transit.
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    (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate
    General Information
    Historical Development
    (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate This compound, traced back to its source, first emerged in the research of past chemistry. In the early years, scholars of chemistry devoted themselves to exploring the properties and changes of various compounds. After long-term research and countless experiments, the synthesis method of this specific structure compound was gradually clarified from the complex chemical synthesis paths. With the passage of time, the technology has become more and more mature, the synthesis efficiency has been improved, and the purity has also improved. From its initial existence as a theoretical concept, to its successful creation, and then to its continuous optimization, the historical evolution of this compound has witnessed the dedication of research in the field of chemistry, laying the foundation for subsequent chemical research and application, and gradually developing its unique value in many fields such as medicine and materials.
    Product Overview
    There is now a substance with the name (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate. This substance has a unique structure and contains a specific spatial configuration. The groups at the 2nd and 3rd positions are arranged in an orderly manner. The configuration of (2R, 3S) determines its chemical properties and reactivity. The fluorine atom with a special phenyl group and 3,5-bis (trifluoromethyl) phenyl at the 2nd position has strong electronegativity, which affects molecular polarity and stability. The 3-fluorophenyl group also contributes to its properties. The 4-methylbenzene sulfonate part can participate in reactions such as ionic bond formation, which affects the solubility and chemical activity of the substance. This substance has potential applications in chemical research, organic synthesis, drug development and other fields, and can be used as a key intermediate to lay the foundation for the creation of new compounds.
    Physical & Chemical Properties
    There is now a substance named (2R, 3S) -2- ((R) -1- (3,5 -bis (trifluoromethyl) phenyl) ethoxy) -3- (4 -fluorophenyl) morpholine 4 -methylbenzene sulfonate. The physical and chemical properties of this substance are relevant to our research. Its properties, melting point, boiling point, and solubility need to be carefully observed. In different solvents, its solubility may vary, or it is easily soluble in a liquid, or it is difficult to melt in other agents. Its stability is also the key. Under different environmental conditions, whether it can maintain its inherent properties and whether there is any risk of decomposition or deterioration. And its density, refractive index and other properties cannot be ignored, which can provide us with important evidence for further investigation of this object, to clarify its essence, and to lay the foundation for subsequent use.
    Technical Specifications & Labeling
    There is now a product with the name (2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine 4 - methylbenzene sulfonate. In this product, technical specifications and identification (product parameters) are the key.
    The preparation of this product should follow precise technical specifications. The choice of raw materials must be high standard, and the ratio must be accurate. For example, the amount of each ingredient is fixed. The temperature and time of the reaction cannot be ignored. If the temperature is high, the substance may change, and if the time is short, it should not be complete.
    On the label, the product parameters should be detailed. From the configuration shown in its chemical structure to the characteristics of the groups contained, it should be clearly marked. Those who see it, that is, its properties and uses are known. In this way, the technical specifications and labels of this thing can be obtained to make a good product.
    Preparation Method
    The method of (2R, 3S) -2- ((R) -1- (3,5 -bis (trifluoromethyl) phenyl) ethoxy) -3- (4 -fluorophenyl) morpholine 4 -methylbenzene sulfonate is related to the raw materials, production process, reaction steps and catalytic mechanism.
    First take the raw material, (3,5 -bis (trifluoromethyl) phenyl) ethanol and suitable halogenated reagents, through substitution reaction, to obtain (R) -1- (3,5 -bis (trifluoromethyl) phenyl) ethoxy halides. At the same time, 4-fluorophenyl morpholine derivatives were prepared. In a suitable solvent, under the action of alkali and catalyst, the key intermediate is obtained through nucleophilic substitution reaction. After reacting with 4-methylbenzenesulfonic acid, the target product is obtained through the salt-forming step. In the
    reaction, it is necessary to precisely control the temperature and time, select a high-efficiency catalyst, and optimize the reaction conditions in each step to increase the purity and yield of the product. This method should be studied more and tried more to improve.
    Chemical Reactions & Modifications
    I am committed to the research of chemical products, and I have worked hard on (2R, 3S) 2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate. Looking at its chemical reaction, think of ways to improve it. Chemical reactions are like changes in yin and yang, subtle and unpredictable. The reaction of this product may not be as subtle as it is, and its mechanism needs to be explored with caution. Hope to understand the mystery, improve the reaction conditions, and make the product purer and more productive. The beauty of chemistry lies in continuous exploration, so that the reaction can be used in a state of perfection, and it can be used as a practical resource in many fields.
    Synonyms & Product Names
    Today there is a thing called (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate. This is a key substance in chemical research.
    Looking for its synonyms and trade names is a treasure in the vast field. Synonyms, or due to different research perspectives and habits, all refer to this specific chemical structure. Trade names are related to commercial operations and are used for product identification in the market.
    Observe this substance, its chemical structure is exquisite and complex, and each group collaborates to give unique properties. In research, the clarity of synonyms and trade names, such as navigation marks. The accurate appellation helps researchers avoid confusion, explore the path of knowledge, accurately connect with the source of raw materials, and deeply analyze the reaction mechanism, so as to achieve the state of scientific research and create a new chapter for chemical research.
    Safety & Operational Standards
    About (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate Safety and Operating Specifications
    Husband (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate, an important substance for chemical research. To properly study this substance, safety and operating standards should be paid attention to first.
    On the safe side, this compound may have specific chemical activities, interact with others, or react biochemically. Therefore, when storing, it must be placed in a cool, dry and well-ventilated place, away from direct sunlight, to prevent deterioration or cause danger. And must be separated from oxidizing, reducing and acid and alkali substances to avoid improper reactions.
    During operation, the researcher must wear appropriate protective equipment. Laboratory clothes, protective gloves and goggles are indispensable to prevent substances from contacting the skin and eyes and causing damage. If operating in a fume hood, ensure normal ventilation and disperse possible harmful gases in time. During operation, the action should be stable and accurate to avoid material spillage. If it is accidentally spilled, clean it up quickly according to the established procedures to prevent pollution of the environment and endanger the safety of personnel.
    Furthermore, the equipment using this compound needs to be regularly calibrated and maintained to ensure accuracy and safety. The reagent should be used in accordance with the regulations and quantitative operations, not more or less. After use, the disposal of the remaining substances should also be carried out according to the regulations and should not be discarded at will. In this way, research can be carried out effectively in a safe environment, the process of chemical exploration can be promoted, and the safety of personnel and the environment can be ensured.
    Application Area
    (The following is described in classical Chinese style about (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate product application field related content)
    There is now a product named (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate. It is in the field of medicine, or can be used as an active ingredient to participate in the development of new agents to treat various diseases. Due to its unique structure, it has potential pharmacological activity, or can regulate the imbalance of human physiology. In the chemical industry, it can be used as a special auxiliary agent to improve material properties and make products more superior. In scientific research experiments, it is a key reagent to help researchers probe the properties of substances and study the principle of reactions. This is the key to its application. With time and in-depth research, it will be able to show extraordinary effects in various fields and contribute to the progress of people's life and science and technology.
    Research & Development
    There is now a product named (2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine - 4 - methylbenzenesulfonate. I am a chemical researcher, focusing on the research and development of this substance.
    This substance has unique characteristics and is of exploration value in the reaction mechanism and application field. After repeated experiments, the relationship between its structure and properties is explored, so as to clarify its reaction law. The research process is full of twists and turns, adhering to the heart of research and making unremitting efforts.
    We hope that through continuous research, we can explore more potential uses for this substance, promote the development of related fields, and contribute to the academic community and industry, so that this substance can bloom in a suitable place and promote further chemical research and application.
    Toxicity Research
    Yu Taste is dedicated to toxicological research, and now focuses on the toxicity of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate. This compound has a unique structure and contains fluorine and trifluoromethyl groups, or has specific effects on biological systems.
    The rest of the thinking, if you want to understand its toxicity, you should study it from multiple ways. First, use cell experiments to observe its effects on different cell lines, observe cell proliferation, apoptosis and morphological changes. Supplemented by animal experiments, measure its half lethal dose, and probe its metabolism and distribution in vivo. And analyze its mechanism of action, and investigate whether it involves specific targets or signaling pathways.
    The road to toxicity research is long, but I must study diligently to obtain the true meaning of toxicity of this compound and provide evidence for its safe application or prevention of harm.
    Future Prospects
    (2R, 3S) -2- ((R) -1- (3,5-Bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate, this is the chemical product I have dedicated myself to studying. Looking to the future, its prospects can be described as vast.
    In the field of pharmaceutical research and development, with its unique chemical structure, it is expected that in-depth investigation will reveal its excellent efficacy for specific diseases. It may be able to accurately act on related targets, bringing new hope to patients.
    In the field of materials science, ingenious modification and improvement may endow materials with unique properties, such as excellent stability and special optical properties, which in turn will promote material innovation and inject new impetus into the development of various industries.
    I firmly believe that with time and unremitting research, this product will surely shine in the future stage of technology and life, and make a unique contribution to human well-being.
    Where to Buy (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate in China?
    As a trusted (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate What is the product?
    There is a substance named\ ((2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) butyl-4-methylbenzenesulfonate\). This is a specific compound in organic chemistry. Its structure is complex and consists of a combination of various groups.
    The name, "\ ((2R, 3S) \) ", indicates the three-dimensional configuration of a specific atom in the compound. " \ (2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) \) ", this part indicates that a specific substituent is attached to the second carbon atom of the main chain. The substituent contains an ethoxy group, and the carbon atom attached to the ethoxy group has a\ ((R) \) configuration, and is connected with\ (3,5-bis (trifluoromethyl) phenyl\)."\ (3- (4-fluorophenyl) \) ", which means that the third carbon atom of the main chain is connected with\ (4-fluorophenyl\). The word" D "indicates that the main chain is a four-carbon chain." \ (4-Methylbenzenesulfonate\) "Then the fourth carbon atom of the main chain of the table is connected to the methylbenzenesulfonate group.
    This compound is used in the field of organic synthesis or has specific uses. It can be used as an intermediate to participate in various reactions to prepare more complex organic molecules. Or because of its unique structure, it also has potential applications in medicinal chemistry, materials science, etc., and can use its special three-dimensional configuration and group properties to achieve specific functions. However, its specific use depends on the relevant research and application scenarios.
    What is the chemical structure of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate?
    Alas! To know the chemical structure of (2R, 3S) - 2 - (R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine - 4 - methylbenzoate, it is necessary to carefully analyze.
    This compound has a complex structure. First of all, its main body is a morpholine ring. At the second position of the morpholine ring, there is a ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) group. In this group, the ethoxy group is attached to the morpholine ring at one end, and the ethyl group at the other end has a substituent of the (R) -configuration, that is, 1- (3,5-bis (trifluoromethyl) phenyl). Among them, 3,5-bis (trifluoromethyl) phenyl means that the 3rd and 5th positions of the benzene ring are each connected with a trifluoromethyl group.
    Look at the 3rd position of the morpholine ring again, which is connected with a 3- (4-fluorophenyl) group, that is, the 4th position of the benzene ring is connected with a fluorine atom. The 4th position of the morpholine ring is connected with a methylbenzoate group. This is after the benzoic acid is estered with methanol, the benzene ring is connected to the 4th position of the morpholine ring.
    In summary, the chemical structure of this compound is composed of a morpholine ring as the core, and multiple different substituents are connected to specific positions on the ring, and each substituent interacts to form its unique chemical structure. Such a complex structure determines its chemical and physical properties, and may have specific uses and reactivity in related chemical fields.
    What are the uses of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
    There is now a product named (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine-4-yl acetate phenyl ester. This substance has a wide range of uses.
    First, it can be used as an active ingredient in the research and development of medicine. The molecular structure is unique, with a specific spatial configuration and chemical group, which can precisely bind to specific targets in organisms, just like the fit of mortise and tenon. Or it can be used to develop drugs for the treatment of specific diseases, such as for some diseases caused by abnormalities of specific biomolecules, through its interaction with the target, it regulates the physiological process in the organism and achieves the purpose of treatment.
    Second, it is also useful in the field of organic synthesis. Because of its complex structure and characteristic groups, it can be used as a key intermediate. Organic synthesis is like building a delicate building block. This intermediate can participate in a variety of chemical reactions by virtue of its functional group characteristics, splicing and combining with other organic molecules to construct more complex and novel organic compounds, opening up new paths for organic synthesis chemistry and enriching the variety of compounds.
    Third, it may have potential value in the field of materials science. In view of its chemical stability and unique physical properties, with appropriate modification and processing, it may be applied to the preparation of materials with special properties. For example, it may endow materials with unique optical and electrical properties, and be applied to optoelectronic devices and other fields, contributing to the development of materials science.
    What is the preparation method of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
    To prepare (2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) butyrolactone - 4 - methylbenzenesulfonate, the method is as follows:
    First take (3,5 - bis (trifluoromethyl) phenyl) ethanol and react with halogenated ethane in a suitable reaction vessel with a suitable base as a catalyst to obtain (R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxyethane. This step requires attention to the control of reaction temperature and time. If the temperature is too high, side reactions will easily occur, and if the time is too short, the reaction may be incomplete.
    Another 4-fluorophenylacetic acid is taken and converted into the corresponding acid chloride through a specific acylation reaction. The acid chloride is reacted with a suitable enol ether to obtain an intermediate product. In this reaction process, the choice of solvent is very critical, and it is necessary to choose one that can promote the reaction without causing too many side reactions.
    Then the (R) -1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxyethane obtained above is reacted with the intermediate product under suitable catalyst and reaction conditions to gradually construct the basic structure of the target molecule. After the reaction is completed, the impurities are removed by separation and purification.
    Finally, the purified product is reacted with methylbenzenesulfonyl chloride, and in a suitable alkaline environment, (2R, 3S) -2- ((R) -1- (3,5 -Bis (trifluoromethyl) phenyl) ethoxy) -3- (4 -fluorophenyl) butyrolactone-4 -methylbenzenesulfonate can be obtained. In this last step of the reaction, the control of the amount of base and the reaction time is related to the purity and yield of the product. The whole preparation process, the conditions of each step of the reaction are finely regulated, and the separation and purification of each intermediate is proper, so that the target product with high purity can be obtained.
    What are the physical and chemical properties of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
    (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine-4-methylbenzoate is an organic compound. Its physicochemical properties are particularly important, related to its performance in various reactions and applications.
    In terms of its physical properties, generally speaking, this compound has a specific melting point and boiling point. The melting point is the critical temperature for the conversion of solid to liquid state, and its value varies depending on the intermolecular force. In this molecule, the presence of aromatic rings and fluorinated groups makes the intermolecular force present a specific state, and the melting point is within a certain range. The boiling point is also affected by the molecular structure. Due to factors such as molecular mass and polarity, it boils at a specific pressure.
    As for chemical properties, this compound contains benzoate ester structure, and the ester group can undergo hydrolysis reaction. Under acidic or basic conditions, the ester bond can be broken to form corresponding acids and alcohols, respectively. And the aromatic ring in the molecule has the typical reactivity of aromatic hydrocarbons, such as electrophilic substitution reaction. Due to the positioning effect of fluorine atoms and trifluoromethyl groups, electrophilic reagents will selectively attack specific positions of aromatic rings. In addition, the morpholine ring also gives it a certain alkalinity and can react with acids to form salts. Its ethoxy group is relatively stable, but it may also undergo chemical transformation under strong oxidation or reduction conditions. The various physical and chemical properties of this compound make it potentially useful in organic synthesis, medicinal chemistry and other fields.