2 2 4 Dinitrophenylthio Benzothiazole
quinoline thiophene imidazole thiazole

2-(2,4-Dinitrophenylthio)benzothiazole

Taiy Chemical

Specifications

HS Code

311186

Chemical Formula C13H7N3O4S2
Molar Mass 347.34 g/mol
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General Information
Frequently Asked Questions
What are the main uses of 2- (2,4-dinitrophenylthio) benzothiazole?
2 - (2,4 -diaminobenzoic acid) benzodiazine is mainly used to play a key role in many fields. In the aerospace field, because of its excellent high temperature resistance, high strength and low density characteristics, it can be used to manufacture key structural components such as wings and fuselages of aircraft, helping to improve the performance and lightweight of aircraft. In the field of electronics and electrical, with its excellent electrical insulation and thermal stability, it is often used in the manufacture of printed circuit boards, electronic packaging materials, etc., to ensure stable and efficient operation of electronic equipment. In the field of automotive manufacturing, due to its good mechanical properties and chemical corrosion resistance, it can be used to manufacture automotive engine peripheral parts, interior parts, etc., which helps to improve the overall quality and durability of automobiles. In the field of composites, composites such as matrix resins and fibers can significantly enhance the performance of composites, and are widely used in construction, sports equipment, and many other aspects, such as the manufacture of high-performance building panels, high-end sports equipment, etc., to meet the needs of different industries for high-performance materials.
What are the synthesis methods of 2- (2,4-dinitrophenylthio) benzothiazole?
2-%282%2C4-%E4%BA%8C%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%A1%AB%E5%9F%BA%29%E8%8B%AF%E5%B9%B6%E5%99%BB%E5%94%91%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E6%9C%89%E5%90%84%E7%A7%8D%E5%BC%82%E5%B7%A5%E5%90%88%E4%BD%9C%E4%B9%8B%E6%96%B9.
First, the precursor of 2 - (2,4-dihydroxybenzoic acid) benzimidazole is the main one. One method can be formed by the condensation reaction of 2-aminobenzimidazole and 2,4-dihydroxybenzoic acid under the action of an appropriate condensing agent. This condensing agent is commonly used, such as dicyclohexyl carbodiimide (DCC), in a suitable organic solvent, such as dichloromethane, N, N-dimethylformamide (DMF), etc., to control the temperature and reaction time, so that the two are condensed and connected to form 2 - (2,4-dihydroxybenzoyl) benzimidazole.
There is another way to protect and activate 2-aminobenzimidazole or 2,4-dihydroxybenzoic acid with appropriate functional groups. For example, the hydroxyl group of 2,4-dihydroxybenzoic acid is protected with a suitable protective group, such as benzyl, and then its carboxyl group is activated, such as conversion to acid chloride, and then reacts with 2-aminobenzimidazole. After the reaction is completed, the protective group is removed, and the target product can also be obtained.
Furthermore, you can try to synthesize it under a catalytic system. Select suitable catalysts, such as some metal complex catalysts, to promote the reaction of the two under mild conditions, improve the reaction efficiency and selectivity, and optimize the yield and purity of the product. Such various methods have their own advantages and disadvantages, and they need to be selected according to the actual situation, such as the availability of raw materials, the ease of control of reaction conditions, and the purity requirements of the product.
What are the physical properties of 2- (2,4-dinitrophenylthio) benzothiazole?
2 - (2,4 -dihydroxybenzoic acid) benzofuranone is a class of organic compounds with special structures. It has attracted much attention in the fields of materials science and medicinal chemistry. Its physical properties are as follows:
1. ** Appearance and properties **: Under normal conditions, it is mostly white to light yellow crystalline powder, which is easy to store and use, and is conducive to uniform dispersion in different reaction systems.
2. ** Melting point and boiling point **: The melting point is usually in a relatively high range, about [X] ° C. A higher melting point indicates that the intermolecular force is strong and the structure is relatively stable. The boiling point is also quite high, which allows the compound to maintain a relatively stable state under high temperature environment, not easy to volatilize, and has obvious advantages in some processes that require high temperature treatment.
3. ** Solubility **: It exhibits good solubility in common organic solvents such as ethanol and acetone, and can form a uniform solution with these solvents, which facilitates its reaction, separation and application in the solution system. However, its solubility in water is poor, which is related to the large proportion of hydrophobic groups in the molecular structure.
4. ** Stability **: Under conventional environmental conditions, 2 - (2,4-dihydroxybenzoic acid) benzofuranone has excellent stability. The benzofuranone skeleton in its structure partially interacts with dihydroxybenzoic acid to enhance the overall stability of the molecule. However, under extreme conditions of strong acids, strong bases or strong oxidants, its structure may be damaged and chemical reactions occur, resulting in changes in properties.
5. ** Spectral properties **: In the ultraviolet-visible spectral region, the compound has a characteristic absorption peak. This is due to the intra-molecular conjugate system, which can absorb specific wavelengths of light and generate electronic transitions. This spectral property is of great significance in the qualitative and quantitative analysis of compounds and their application as optical materials. Its content and purity can be accurately determined by spectral analysis.
What are the chemical properties of 2- (2,4-dinitrophenylthio) benzothiazole?
2- (2,4-diaminobenzoic acid) benzodiazine is a class of compounds with unique properties. Its chemical properties are rich and diverse, and it has important applications in many fields.
First of all, 2- (2,4-diaminobenzoic acid) benzodiazine contains active functional groups and can exhibit excellent reactivity. Under heating conditions, benzodiazine rings can be ring-opened polymerized, and three-dimensional cross-linked structures can be formed through this process. This property makes it very useful in the preparation of high-performance thermosetting resins. Due to the fact that no small molecules are released during ring-opening polymerization, the formed polymer has excellent mechanical properties, such as high strength and modulus, and is very popular in fields such as aerospace and automobile manufacturing that require strict mechanical properties of materials.
Secondly, the benzene ring structure in 2 - (2,4-diaminobenzoic acid) benzodiazine gives it good thermal stability. The polymer can withstand high temperatures and has a high thermal decomposition temperature. It can still maintain structural stability and good performance in high temperature environments, which makes it suitable for insulating materials and high temperature resistant coatings in high temperature environments.
Furthermore, the molecular structure of the compound can be flexibly adjusted by modifying the 2,4-diaminobenzoic acid part. Different substituents can be introduced to change its solubility, reactivity and final properties of the polymer, so as to achieve precise regulation of material properties to meet the needs of different application scenarios.
In addition, 2 - (2,4 - diaminobenzoic acid) benzodiazine may also have certain chemical resistance. Due to its cross-linking structure and special molecular configuration, it is resistant to some chemical substances and is suitable for some occasions that require contact with chemical media, such as chemical equipment linings.
What are the precautions for 2- (2,4-dinitrophenylthio) benzothiazole during use?
2-%282%2C4-%E4%BA%8C%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%A1%AB%E5%9F%BA%29%E8%8B%AF%E5%B9%B6%E5%99%BB%E5%94%91, when taking medicine, you need to pay attention to many matters.
First, when the syndrome is distinguished, although this medicine is good, if the syndrome type does not match, rashly use it, not only difficult to obtain its effect, but also harmful. Only by carefully reviewing the patient's symptoms, signs, tongue, pulse, etc., and accurately differentiating the syndrome, can it be used properly.
Next, pay attention to the dose. If the medication is used in the military, the dose is very important. The dose of 2-%282%2C4-%E4%BA%8C%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%A1%AB%E5%9F%BA%29%E8%8B%AF%E5%B9%B6%E5%99%BB%E5%94%91 must be carefully weighed according to the patient's age, constitution, severity of illness and other factors. For children, the elderly and the infirm, the dose should be reduced; for young and strong and seriously ill, it may be slightly increased, but it should not exceed the safe range.
Furthermore, during the medication period, the diet should also be cautious. Spicy, greasy, raw and cold things can easily disturb the spleen and stomach, or interact with the drug, affecting the efficacy of the drug. Therefore, it is advisable to eat a light diet to help the drug exert its power.
Repeat, pay attention to the adverse reactions of the drug. After medication, closely observe your own reaction. If you see discomfort such as rash, itching, nausea, vomiting, and dizziness, you should immediately stop the drug and seek medical consultation. Do not be negligent and delay the condition.
In addition, if you are using other drugs, you must inform the doctor. There may be interactions between drugs, which may increase the efficacy or increase the risk. The doctor knows the whole picture of the medication, so he can weigh the pros and cons and ensure the safety of the medication.
In short, with 2-%282%2C4-%E4%BA%8C%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%A1%AB%E5%9F%BA%29%E8%8B%AF%E5%B9%B6%E5%99%BB%E5%94%91, be careful and follow your doctor's advice, so that you can play well and keep safe.