What is the chemical structure of 4-chloro-2 - [5-hydroxy-3-methyl-1 - (3-sulfophenyl) pyrazole-4-ylazo] - 5 -methylbenzenesulfonate calcium salt
This compound is named 4 + -cyano- 2 - [5 - hydroxymethyl - 3 - methyl - 1 - (3 - pyridyl) piperidine - 4 - yl] - 5 - methylpyridine - 2 - carboxylic acid amide, and its chemical structure is analyzed as follows:
From the main structure, the compound has a pyridine ring structure. The pyridine ring is a six-membered nitrogen-containing heterocyclic ring, which has certain aromaticity and stability. It provides a basic skeleton and chemical activity check point for the whole molecule.
There is a complex side chain connected at position 2 of the pyridine ring. This side chain starts from a piperidine ring. The piperidine ring is a six-membered nitrogen-saturated heterocycle. Its position 1 is connected to a 3-pyridyl group, giving the molecule more conjugated structure and potential biological activity. The position 3 of the piperidine ring is connected to methyl group, which acts as a common alkyl substituent and can affect the lipid solubility and steric resistance of the molecule. The position 5 is connected to hydroxymethyl group. The presence of hydroxyl group increases the hydrophilicity of the molecule, while methyl group retains a certain lipid solubility. This combination makes the molecule reach a certain balance between hydrophilicity and lipid solubility. Position 4 is connected to the pyridine ring, which firmly binds the side chain of the piperidine ring to the main chain of the pyridine ring. Position 4 of the
pyridine ring is connected to the cyano group, which has strong electron-absorbing properties and can change the electron cloud distribution of the pyridine ring, which in turn affects the chemical activity and reactivity of the whole molecule. Position 5 is connected to the methyl group, which further changes the electron cloud density and spatial structure of the pyridine ring. In addition to connecting the above side chains, the No. 2 position of the
pyridine ring is also connected with a carboxyamide group. The carbonyl group in the carboxyamide group forms a conjugated structure with the amino group, which has certain stability. At the same time, the amino group and the carbonyl oxygen atom can participate in the formation of hydrogen bonds, which affects the crystal structure, solubility and interaction with biological macromolecules of the molecule.
The interaction of various groups in the structure of this compound endows it with unique physical and chemical properties and potential biological activities, and may have important research value and application prospects in the fields of medicinal chemistry.
What are the uses of 4-chloro-2 - [5-hydroxy-3-methyl-1 - (3-sulfophenyl) pyrazole-4-ylazo] - 5 -methylbenzenesulfonate calcium salt
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What are the physical properties of calcium 4-chloro-2 - [5-hydroxy-3-methyl-1 - (3-sulfophenyl) pyrazole-4-ylazo] - 5 -methylbenzenesulfonate?
5-Methyl-2 - [5-amino-3-methyl-1 - (3-pyridyl) - 4-piperidinyl] - 5-methylpyridine-3-formic acid amide, this material is complex, let me come one by one.
Its appearance is often white to off-white crystalline powder, the texture is delicate and uniform, and the color is stable under certain light and environment, and there is no obvious discoloration.
In terms of solubility, in organic solvents, such as methanol, ethanol and other common alcohols, it has a certain solubility and can slowly dissolve to form a uniform solution. However, the solubility in water is relatively limited and only slightly soluble. This property is related to the hydrophilicity and hydrophobicity of the groups contained in the molecular structure. Many organic groups have a hydrophobic tendency, so they do not dissolve well in water.
In terms of stability, under conventional temperature and humidity environments, the properties are relatively stable, and there is no obvious spontaneous decomposition or deterioration phenomenon. However, in extreme chemical environments such as strong acids and strong bases, some chemical bonds in its structure may be affected, and reactions such as hydrolysis and substitution occur, causing molecular structure changes, affecting its chemical properties and efficacy.
In terms of melting point, it has been determined to be within a specific temperature range, which is of great significance for its identification and purity determination. When heated to this temperature, the substance gradually melts from solid to liquid, and the phase transition process is relatively stable, reflecting the characteristics of intermolecular forces.
As for its performance in chemical reactions, because its structure contains a variety of active groups, such as amino groups, pyridyl groups, etc., it can be used as nucleophilic reagents or electrophilic reagents to participate in many organic reactions, showing rich chemical activity and wide use in the field of organic synthesis.
What is the preparation method of 4-chloro-2 - [5-hydroxy-3-methyl-1 - (3-sulfophenyl) pyrazole-4-ylazo] - 5 -methylbenzenesulfonate calcium salt
To prepare 4 + -alkane-2- [5-hydroxymethyl-3-methyl-1- (3-hydroxyphenyl) piperidin-4-ketoxy] -5-methylbenzene hydroxylic anhydride, the method is as follows:
First take an appropriate amount of starting materials, and mix the compounds containing specific groups in appropriate proportions. In a suitable reaction vessel, create a stable reaction environment, and the conditions such as temperature and pressure need to be precisely controlled.
The first step is to carefully select suitable reagents to react with the 5-hydroxymethyl-3-methyl-1- (3-hydroxyphenyl) piperidine moiety to promote its structure transformation as expected. This process requires close attention to the reaction process and monitoring the degree of reaction by means such as thin-layer chromatography to ensure that the reaction is sufficient and not excessive.
In the next step, the product treated in the first step is combined with the reactants related to 4 + -alkane-2 - and ketooxygen. By skillfully adjusting the reaction conditions, such as selecting suitable catalysts, the two can be effectively combined to produce a specific chemical reaction, and the prototype of the target product is gradually constructed.
Furthermore, for the part of 5-methylphenylhydroxylic anhydride, the reaction system is introduced at an appropriate stage, and various organic reaction mechanisms, such as acylation reaction, are used to make it reasonably integrated into the overall molecular structure to complete the construction of the final product.
After the reaction is completed, the impurities are removed through fine operations such as separation and purification to obtain pure 4 + -alkane-2 - [5-hydroxymethyl-3-methyl-1 - (3-hydroxyphenyl) piperidine-4-ketoxy] - 5-methylbenzene hydroxyanhydride products. The whole process is crucial to control the reaction conditions, raw material ratio and operation steps. It is difficult to obtain the ideal product with a little difference.
4-Chloro-2 - [5-hydroxy-3-methyl-1 - (3-sulfophenyl) pyrazole-4-ylazo] - 5 -methylbenzenesulfonate calcium salt What are the precautions during use
The combination of saltpeter, sulfur, and charcoal into gunpowder is a major invention in ancient China. In the process of using gunpowder, many matters must be paid attention to.
First, be careful with raw materials. Saltpeter, sulfur, etc. are all dangerous things and have strong properties. If they are not properly stored, they will be heated, damp, or mixed with other things improperly, which can easily lead to accidents. As the "Remarks" states, choose a dry, cool and ventilated place, and separate the raw materials properly to prevent deterioration and accidents.
Second, accurate proportions. The power of gunpowder depends on the accurate ratio of saltpeter, sulfur, and charcoal. Saltpeter is the king, and the main power of ignition and explosion; sulfur supports combustion, increasing its speed; charcoal adjusts to stabilize combustion. The proportion is slightly poor, or the power is insufficient, or the explosion is disorderly. Ancient alchemists and craftsmen, after countless trials, have a delicate ratio, and the user should not be careless.
Third, manage the environment. Preparation and use of gunpowder, must avoid open flames and static electricity. The place should be spacious, free of debris accumulation, and well ventilated to prevent the accumulation of poisonous gases. And the operator, in front of cotton clothes, remove metal accessories to prevent static electricity from igniting fire.
Fourth, use it to a certain extent. Gunpowder is a sharp weapon and can be used in warfare and fireworks. However, it should be used in accordance with morality. It should not be used indiscriminately to kill innocent people, nor should it be used indiscriminately in places where fire is prohibited, causing fire and man-made disasters.
In general, although gunpowder is powerful and beneficial to mankind, those who use it must be in awe and cautious in order to ensure safety and benefit the country and the people.