As a leading (2R,4R) Cis-(2,4-Dichlorophenyl)-2-(1,2,4-Triazole-1-Yl-Methyl)-1,3-Dioxolane-4Yl-Methyl-P-Tolysulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
(2R, 4R) Cis- (2,4 -dichlorophenyl) -2 - (1,2,4 -triazole-1 -ylmethyl) -1,3 -dioxolane-4 -ylmethyl What are the chemical properties of p-toluenesulfonate
(2R, 4R) cis- (2,4-dihydroxyphenyl) -2- (1,2,4-triazine-1-ylmethyl) -1,3-dioxane-4-ylmethyl-p-toluenesulfonate This compound has unique chemical properties. It exhibits a variety of properties due to the presence of multiple special groups in its structure.
First, the chiral center (2R, 4R) endows it with stereochemical characteristics, which affect its arrangement and interaction in space. When it binds to specific chiral receptors or participates in chiral catalytic reactions, it can determine the stereoselectivity and activity of the reaction.
Furthermore, dihydroxyphenyl groups provide hydrophilicity and certain reactivity. Hydroxyl groups can participate in the formation of hydrogen bonds, enhance the interaction with polar molecules or surfaces, and can also undergo reactions such as esterification and etherification, which change the physicochemical properties and biological activities of molecules.
The triazinyl methyl moiety has strong electronic effects and conjugated structures, which affect the electron cloud distribution and stability of molecules. Triazine rings can participate in a variety of heterocyclic reactions, introduce more functional groups, and expand their chemical uses.
The dioxane heterocyclic structure gives molecules a specific ring tension and spatial conformation, which affects the stability and reactivity of molecules. It can be used as a potential reaction check point or protective group in some reactions.
p-toluenesulfonate is a good leaving group, which is easily replaced by other nucleophiles in nucleophilic substitution reactions. It is often used to construct new carbon-carbon and carbon-heteroatomic bonds, so as to realize the structural modification and functionalization of molecules.
This compound has potential application value in organic synthesis, pharmaceutical chemistry and other fields due to the synergistic effect of these groups. It can be used as a key intermediate for the synthesis of compounds with specific biological activities or for the design of new materials.
(2R, 4R) Cis- (2,4 -dichlorophenyl) -2 - (1,2,4 -triazole-1 -ylmethyl) -1,3 -dioxolane-4 -ylmethyl What are the main uses of p-toluene sulfonate
(2R, 4R) cis- (2,4-dihydroxyphenyl) - 2 - (1,2,4-triazine-1-ylmethyl) - 1,3-ring-dioxide-4-methylphenyl-p-toluenesulfonate This compound has a wide range of uses. It is often used as a key intermediate for active pharmaceutical ingredients in the field of medicine. Due to its special chemical structure, it can participate in a variety of chemical reactions. It can be skillfully modified and transformed to generate compounds with specific pharmacological activities for the development of new drugs and the treatment of various diseases.
It also has important functions in the field of materials science. It can be used as a building block of functional materials. By polymerizing or cross-linking with other compounds, it imparts unique properties to the material, such as improving the stability, solubility or optical properties of the material, and contributes to the creation of high-performance new materials.
Furthermore, in the field of organic synthetic chemistry, it is an important synthetic building block. Chemists can use it as a starting material and use various organic reactions to build complex organic molecular structures, expand the boundaries of organic synthesis, and help create new organic compounds. Promote the development of organic chemistry.
Because of the cooperation of functional groups in its structure, it gives this substance a variety of reactivity and application potential. It plays an indispensable role in the above fields and has become an important compound in scientific research and industrial production.
(2R, 4R) cis- (2,4 -dichlorophenyl) -2 - (1,2,4 -triazole-1 -ylmethyl) -1,3 -dioxolane-4 -ylmethyl What is the preparation method of p-toluene sulfonate
To prepare (2R, 4R) cis- (2,4-dihydrobenzyl) -2- (1,2,4-triazine-1-ylmethyl) -1,3-ring dioxide-4-ylmethylbenzyl-p-toluenesulfonate, the method is as follows:
First take an appropriate amount of raw materials and follow a specific reaction sequence and conditions. The first step is to prepare the (2R, 4R) cis-structural part. This step requires fine control of the reaction environment, such as temperature, pH, etc., so that the reaction proceeds in the desired three-dimensional configuration direction. For the introduction of dihydrobenzyl, when finding a suitable reaction reagent and reaction path, or borrowing nucleophilic substitution and other reaction mechanisms, it is precisely connected to the target position.
When preparing the 1,2,4-triazine-1-ylmethyl moiety, it is also necessary to select suitable starting materials according to its chemical properties, and through a series of reactions, form a stable triazine structure and connect it to a specific position.
As for the construction of the 1,3-dioxide ring-4-ylmethylbenzyl moiety, attention should be paid to the selectivity and yield of the reaction. This complex structure can be built step by step through a multi-step reaction, each step of which requires careful operation to ensure the purity and structural correctness of the product.
Finally, p-toluenesulfonate is introduced. This step needs to consider the activity and selectivity of the reaction, so that it can be smoothly combined with the constructed main structure to generate the target product. During the whole process, it is necessary to closely monitor the reaction process and use suitable analytical methods, such as thin layer chromatography, nuclear magnetic resonance, etc., to control the quality and purity of the product, so as to obtain the required (2R, 4R) cis- (2,4-dihydrobenzyl) -2- (1,2,4-triazine-1-ylmethyl) -1,3-ring dioxide-4-ylmethylbenzyl-p-toluenesulfonate.
(2R, 4R) Cis- (2,4 -dichlorophenyl) -2 - (1,2,4 -triazole-1 -ylmethyl) -1,3 -dioxyamyl-4 -ylmethyl p-toluenesulfonate What is the price range in the market?
(2R, 4R) cis- (2,4-dihydroxyphenyl) - 2 - (1,2,4-triazine-1-ylmethyl) - 1,3-ring dioxide-4-ylmethyl-p-toluenesulfonate, the price range of this product on the market is difficult to say exactly. The price of the cover often varies due to many factors, such as the abundance of raw materials, the difficulty of preparation, the amount of market demand, and the quality of the process.
Looking at the market conditions in the past, if the raw materials are sufficient, the preparation process is mature and the market demand is stable, the price may hover in a certain range. However, if the raw materials are scarce, it takes a lot of material resources and manpower to find them, or the preparation process is complicated, requires multiple fine processes, time-consuming and laborious, and the price will rise.
And market demand is also the key. If there is a large demand for this product in a certain industry, and the supply is in short supply, its price will also rise. On the contrary, if there is little demand, merchants may reduce prices to reduce inventory.
In addition, the price varies from region to region and season to season. Therefore, in order to determine its price range in the current market, it is necessary to carefully observe the dynamics of the current market, consult industry experts, or refer to recent transaction data to obtain a relatively accurate number, but it is only a temporary price, which is difficult to become a constant fixed number.
(2R, 4R) cis- (2,4-dichlorophenyl) -2 - (1,2,4-triazole-1-ylmethyl) -1,3-dioxolane-4-ylmethyl What are the precautions in the use of p-toluene sulfonate
(2R, 4R) Formula - (2,4 - diazolyl) - 2 - (1,2,4 - triazolyl - 1 - methyl) - 1,3 - dioxy - 4 - methylnaphthalene - methylnaphthalenesulfonate During use, pay attention to the following things:
First, this compound is, before use, it must be clear its refining properties. because it contains multi-functional groups, such as diazolyl, triazolyl, dioxy and sulfonate groups, etc., each functional group affects each other, and its chemical activity and reaction properties also affect each other. Therefore, it is necessary to study its physicochemical properties, such as melting, boiling, solubility, etc., in order to operate the dissolution and dissolution of the compound.
Second, note its characterization. Sulfonate-based phase is active, and under different degrees, pH values and dissolution environments, it may cause reactions such as hydrolysis and elimination. Especially in high-temperature, high-temperature or acidic components, it is necessary to pay more attention to their characterization. Storage should be placed in dry, dry and sealed environments to prevent reactions such as moisture and air.
Third, consider the reactivity of reactivity. Multiple active sites in the molecule may cause side reactions to occur. In synthesis or other chemical reactions, careful reactivity and catalysis are required to improve the reactivity of the target. For example, control the reaction rate, reaction rate and reaction rate, so that the reaction rate may go in the desired direction, reduce unnecessary side effects, and improve the reaction rate.
Fourth, safety precautions should not be ignored. Do not consider the toxicity and irritation of the compound itself, and pay attention to whether its decomposition or reaction effects are harmful. Operate well, follow the relevant safety procedures, and wear anti-corrosion protection, such as gloves, eyes, masks, etc. If used in an undesirable environment, pay attention to pass safety to avoid harmful steaming.