2 Aminobenzo D Thiazole 6 Carbonitrile
Quinoline Thiophene Imidazole Thiazole
2-Aminobenzo[d]thiazole-6-carbonitrile
Chemical Formula C8H5N3S
Molar Mass 175.21 g/mol
Appearance Solid (usually powder)
Melting Point Data may vary, typically in a specific temperature range
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some organic solvents like DMSO, DMF
Pka Related to its acidic or basic nature in solution, specific value depends on conditions
Uv Vis Absorption Exhibits characteristic absorption bands in the UV - Vis spectrum
FAQ

What are the chemical properties of 2-Aminobenzo [d] thiazole-6-carbonitrile

2-Aminobenzo [d] thiazole-6-formonitrile is one of the organic compounds. Its chemical properties are profound, and I would like to describe them in detail.

As far as its physical properties are concerned, this compound is usually in a solid state, and its melting point, boiling point and other properties are closely related to the arrangement and interaction of atoms in the molecule. The amino (-NH2O), cyano (-CN) and benzothiazole ring structures contained in the molecule give it unique properties.

Amino groups have certain alkalinity and can react with acids to form corresponding salts. This is because there are lone pairs of electrons on nitrogen atoms, which can accept protons. The cyanyl group is a strong electron-absorbing group, which has a great influence on the electron cloud distribution of the molecule, resulting in a certain polarity of the molecule.

Furthermore, the conjugated system of benzothiazole ring makes the molecule stable to a certain extent and affects its spectral properties. In chemical reactions, the amino group of 2-aminobenzo [d] thiazole-6-formonitrile can participate in many nucleophilic reactions, such as acylation with acyl halides, acid anhydrides, etc., to form amide derivatives.

Cyanyl groups can also participate in various reactions, such as hydrolysis to carboxyl groups under appropriate conditions, or addition reactions with nucleophiles. The part of benzothiazole ring can participate in the substitution reaction on the ring. Due to the different electron cloud densities at different positions on the ring, the activity and check point of the substitution reaction are also different.

Its solubility is affected by molecular polarity and structure. It may have good solubility in polar organic solvents such as dimethyl sulfoxide (DMSO) and N, N-dimethylformamide (DMF), but poor solubility in non-polar solvents.

This compound has a wide range of uses in the field of organic synthesis and is often an important intermediate for the synthesis of complex organic molecules. Its unique chemical properties provide many possible avenues for organic synthesis chemistry.

2-Aminobenzo [d] What are the main uses of thiazole-6-carbonitrile

2-Aminobenzo [d] thiazole-6-formonitrile has a wide range of uses in the field of organic synthesis. First, it can be used as a key intermediate for the creation of new drugs. In the way of pharmaceutical research and development, by modifying and modifying its structure, compounds with unique biological activities can be obtained, which are expected to become good drugs against specific diseases. For example, through a specific reaction, adding a specific functional group may enhance its affinity to a specific target, thereby enhancing the efficacy.

Second, it also plays an important role in the creation of pesticides. Using this as a starting material, pesticides with high insecticidal, bactericidal or herbicidal activities can be synthesized. Due to the particularity of the structure of the compound, it may endow the pesticide with a unique mechanism of action, which can deal with the existing pesticide resistance problems and provide new paths for the prevention and control of agricultural pests, diseases and weeds.

Third, it has also shown its presence in the field of materials science. Or it can participate in the preparation of materials with special photoelectric properties, such as organic Light Emitting Diode (OLED) materials. Because of the specific atomic and chemical bond arrangement in its molecular structure, it may affect the electronic transport and luminescence properties of the material. After rational design and synthesis, it may contribute to the development of OLED technology, making display devices more high definition and energy saving.

Fourth, in the field of dye chemistry, based on this, new functional dyes may be developed. With its structural characteristics, the color, stability and affinity of dyes to different substrates can be adjusted, and it has potential applications in textile, printing and dyeing industries. It can make the dyeing process more environmentally friendly and efficient, and the color performance is richer.

What is the synthesis method of 2-Aminobenzo [d] thiazole-6-carbonitrile

The synthesis method of 2-aminobenzo [d] thiazole-6-formonitrile, let me tell you in detail.

First, the commonly used synthesis path is to start with benzothiazole derivatives containing specific substituents. First take a suitable benzothiazole, which must have reactive functional groups at specific positions, such as halogen atoms or other active groups.

Taking halogenated benzothiazole as an example, it can undergo nucleophilic substitution with cyanide reagents. This cyanide reagent, such as potassium cyanide, sodium cyanide and other metal cyanides, under appropriate reaction conditions, the cyanyl group can replace the halogen atom, thereby introducing the cyanyl functional group at the specific position of benzothiazole to obtain the cyanide-containing benzothiazole intermediate.

Then, the amination modification of the intermediate is also a key step. The intermediate is often aminated by an ammonia source, such as ammonia gas, ammonia water or amine compounds, under suitable catalysts and reaction conditions. The catalyst can be selected from a catalytic system composed of transition metal catalysts and their ligands. By catalysis, ammonia sources react with intermediates, and amino groups are introduced at specific positions of benzothiazole to obtain the final target product 2-aminobenzo [d] thiazole-6-formonitrile.

In addition, the control of reaction conditions is extremely important. Temperature needs to be precisely regulated, and the temperature required for different reaction steps varies. During nucleophilic substitution reactions, the temperature may need to be maintained within a specific range to ensure the reaction rate and selectivity. The same is true for amination reactions. Too high or too low temperature may affect the reaction process and product yield.

Furthermore, the choice of reaction solvent cannot be ignored. Suitable solvents must have good solubility to the reactants and do not side-react with the reactants and products. Common organic solvents such as dimethylformamide and dichloromethane can be selected according to the specific reaction steps and the characteristics of the reactants.

In short, by reasonably designing the reaction route, precisely controlling the reaction conditions and solvent selection, 2-aminobenzo [d] thiazole-6-formonitrile can be effectively synthesized.

2-Aminobenzo [d] thiazole-6-carbonitrile price in the market

What is the price of 2-aminobenzo [d] thiazole-6-formonitrile in the market? I have carefully reviewed "Tiangong Kaiwu", but I have not obtained the price of this substance. This is an important intermediate in organic synthesis and is widely used in medicine, pesticides, materials and other fields. However, "Tiangong Kaiwu" was written in the Ming Dynasty, when the technology of chemical synthesis was not yet developed, and it was difficult to describe its price.

At present, the price of this chemical varies depending on the purity, manufacturer, and market supply and demand. High purity, the price may be high; if mass production and oversupply, the price may be lower. For accurate prices, you can consult chemical reagent suppliers, or check on chemical product trading platforms. The price information that changes from time to time can enable you to obtain the current market price of this product.

2-What are the manufacturers of Aminobenzo [d] thiazole-6-carbonitrile

Today I have a question, the geometry of the manufacturer of 2 - Aminobenzo [d] thiazole - 6 - carbonitrile. This is an organic compound, which is widely used in medicine, pesticides and other fields.

In China, there are many manufacturers producing this compound. For example, some manufacturers in Jiangsu have profound chemical industry heritage and exquisite technology. The quality of this product produced is high, and it is supplied to all parties. Furthermore, there are also manufacturers involved in Shandong, where the chemical industry is developed, the resources are rich, the production process is constantly refined, and the products are also competitive.

Overseas places, Europe and the United States also have related manufacturers. Its scientific research strength is strong, and it has been studying in the field of organic synthesis for many years. Its production technology is advanced, and the product specifications are diverse, which can meet the needs of different customers around the world. < Br >
However, if you want an accurate and complete list of manufacturers, you can visit the chemical industry information platform, professional exhibition directory, or consult the chemical industry association, so that you can obtain detailed information, comprehensive and without omission.