2- {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutan-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,3-benzothiazole-7-sulfonic What is the chemical structure of acid
This is the naming of an organic compound. To clarify its chemical structure, it is necessary to analyze it according to the naming rules of organic chemistry. Its name is long and complicated, containing many functional groups and substituent information.
The main part of the first view, "1,3-benzothiazole-7-sulfonic acid", this is the parent nuclear structure, that is, benzothiazole ring, and has a sulfonic acid group at position 7.
Look again at the substituent, "2 - {4- [ (E) - {1 - [ (2 -methoxyphenyl) amino] -1,3 -dioxidine-2-yl} diazo] -3 -sulfophenyl} -6 -methyl". " 6-Methyl "indicates that there is a methyl substitution at the 6th position of the benzothiazole ring;" 2 - {4- [ (E) - {1 - [ (2-methoxyphenyl) amino] -1,3-dioxidine-2-yl} diazo] -3-sulfophenyl} "In this part, there is a complex substituted phenyl group attached to the 2nd position of the benzothiazole ring, and the 4th position of the phenyl group is connected by a diazo group to another structure, which is" 1 - [ (2-methoxyphenyl) amino] -1,3-dioxidine-2 " -Group ", and the third position of the phenyl group also has a sulfonic acid group.
In general, the chemical structure of this compound is composed of a benzothiazole parent nucleus, together with a sulfonic acid group, a methyl group, and a substituted phenyl group containing complex functional groups such as diazo, methoxyphenylamino, and dioxybutyl. This complex structure and the interaction of functional groups endow the compound with unique chemical and physical properties.
2- {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutan-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,What are the main uses of 3-benzothiazole-7-sulfonic acid
2-% {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutyl-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,3-benzothiazole-7-sulfonic acid is an organic compound. However, in the category of ancient processes and creations involved in "Tiangong Kaiwu", such modern compounds with complex chemical structures are rarely seen. This compound is mostly used in modern chemistry and specific fields of chemical industry.
In modern chemical research, this compound may be used for the preparation of dyes due to its unique structure and properties. It contains diazoenyl groups and sulfonic acid groups, etc. Diazoenyl groups can give color to dyes, and sulfonic acid groups can enhance water solubility, making dyes better disperse and adhere to fabrics. It is widely used in the textile printing and dyeing industry to dye fabrics with rich colors.
In the field of biochemical analysis, this compound may be used as an analytical reagent. Due to its special chemical structure, it can react with specific biomolecules. By observing the reaction phenomenon or detecting the product, the qualitative and quantitative analysis of biomolecules can be realized, which helps life science research and medical diagnosis.
Or it has applications in materials science. Using its chemical properties, the surface of the material is modified to improve the surface properties of the material, such as hydrophilicity, biocompatibility, etc., so that the material can achieve better application results in biomedical materials, electronic materials and other fields. Although this object is not listed in Tiangong Kaiwu, the development of modern science and technology has given it important applications in many fields, promoting the progress of chemical, biological, materials and other disciplines.
2- {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutan-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,3-benzothiazole-7-sulfonic What are the physical properties of acid
This compound is named 2 - {4 - [ (E) - {1 - [ (2 - methoxyphenyl) amino] -1,3 - dioxidine - 2 - yl} diazo] -3 - sulfophenyl} -6 - methyl - 1,3 - benzothiazole - 7 - sulfonic acid. Due to its complex structure, there is no record of the physical properties of this kind of compound in "Tiangongkai". The following is based on modern chemical knowledge and is explained to you in a similar way to ancient classical expressions:
This compound contains a special structure and is connected by benzothiazole, phenyl and other parts. In terms of physical properties, due to the sulfonic acid group, it may have a certain solubility in water. The sulfonic acid group is a hydrophilic group, which can make the compound more easily dispersed in polar solvents. Its appearance may be solid, and it forms a tight structure due to the interaction between atoms in the molecule. And because of the conjugated system containing benzene rings and other conjugated systems, or having a certain color, the conjugated structure will absorb visible light of specific wavelengths, causing it to appear colored.
At the same time, there are diazo groups in the molecule, which are active and may affect the stability of the compound. And groups such as methoxy and dioxobutyl will also play a role in the overall physical properties. Methoxy group power supply effect, or changes the distribution of molecular electron clouds, which affects the way it interacts with other
2- {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutan-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,3-benzothiazole-7-sulfonic What is the synthesis method of acid
To prepare 2 - {4 - [ (E) - {1 - [ (2 -methoxyphenyl) amino] -1,3 -dioxidine-2-yl} diazenyl] -3 -sulfonylphenyl} -6 -methyl-1,3 -benzothiazole-7 -sulfonic acid, the synthesis method is as follows.
Take 2-methoxyaniline first and make it react with succinic anhydride in a suitable reaction environment to obtain 1 - [ (2-methoxyphenyl) amino] -1,3 -dioxidine-2 -acid. This reaction needs to be controlled by temperature and time, so that the two can fully react to obtain a higher yield.
Then the obtained 1- [ (2-methoxyphenyl) amino] -1,3-dioxodine-2-acid is diazotized in an acidic environment with suitable diazotizing reagents, such as sodium nitrite, to obtain the corresponding diazonium salt. In this process, the type, concentration, and reaction temperature of the acid need to be precisely controlled to avoid the decomposition of the diazonium salt.
Take another 3-amino-4-sulfobenzoic acid and couple it with the above diazonium salt to form 2 - {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxydino-2-yl} diazenyl] -3 -sulfobenzoic acid}. During the reaction, attention should be paid to the reaction conditions to make the coupling reaction proceed smoothly.
Subsequently, the product is reacted with suitable sulfur-containing reagents, such as thiourea, etc., under specific conditions, and the benzothiazole structure is introduced to generate 2 - {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3 -dioxydinyl-2-yl} diazenyl] -3 -sulfonylphenyl} -6 -methyl-1,3 -benzothiazole-7 -sulfonic acid. The reaction conditions of this step, such as temperature, reaction time, and reagent dosage, all have important effects on the purity and yield of the final product, so caution is required. After each step of the reaction, it should be separated and purified by methods such as recrystallization and column chromatography to obtain a pure product.
2- {4- [ (E) - {1- [ (2-methoxyphenyl) amino] -1,3-dioxobutan-2-yl} diazenyl] -3-sulfophenyl} -6-methyl-1,3-benzothiazole-7-sulfonic acid What are the precautions during use
This is 2 - {4 - [ (E) - {1 - [ (2 - methoxyphenyl) amino] - 1,3 - dioxidine - 2 - yl} diazo] - 3 - sulfonylphenyl} - 6 - methyl - 1,3 - benzothiazole - 7 - sulfonic acid, which in the process of use, there are many points to pay attention to.
bear the brunt, this compound contains diazo groups, active properties, poor stability, heat, light or specific chemicals, easily lead to decomposition or other chemical reactions. Therefore, it is necessary to store it in a cool, dry and dark place to prevent it from deteriorating and affecting the use effect.
Furthermore, the presence of sulfonic acid groups and sulfonyl groups makes the compound acidic. During operation, avoid contact with alkaline substances to avoid neutralization reactions, damage the molecular structure, and change its chemical properties. Moreover, acidic conditions may corrode certain materials. When using, suitable containers and tools should be selected, such as acid-resistant glassware or specific plastic products, to prevent the container from being corroded and causing the compound to be contaminated.
In addition, this compound has a complex structure and contains multiple functional groups, and different groups may occasionally affect each other's reactivity. When participating in a chemical reaction, it is necessary to carefully control the reaction conditions, such as temperature, pH, reaction time, etc., to ensure that the reaction proceeds in the expected direction and avoid the occurrence of side reactions.
At the same time, in view of its complex structure, its solubility may have special requirements. Before use, it is necessary to clarify its dissolution in different solvents, select a suitable solvent to achieve the best dissolution effect, and then ensure its dispersion and uniformity in the reaction system or application scene.
Finally, the compound may have certain biological activity and toxicity. When operating, it is necessary to strictly follow the safety operating procedures, wear necessary protective equipment, such as gloves, goggles, masks, etc., to prevent contact with the skin, inhalation or ingestion, and ensure the safety of experimenters.