Benzothiazole 2 Thiol
Quinoline Thiophene Imidazole Thiazole
Benzothiazole-2-thiol
Chemical Formula C7H5NS2
Molar Mass 167.25 g/mol
Appearance Yellow - white crystalline solid
Odor Characteristic unpleasant odor
Melting Point 167 - 171 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in ethanol, acetone, benzene
Acidity Pka Around 3.5
Flash Point 170 °C
Stability Stable under normal conditions, but can react with strong oxidizing agents
FAQ

What are the main uses of Benzothiazole-2-thiol?

Benzothiazole-2-mercaptan is one of the organic compounds with a wide range of uses. In the field of medicine, it is often a key intermediate for the synthesis of many drugs. The special chemical structure of Gain benzothiazole-2-mercaptan can be combined with specific targets in organisms or participate in biochemical reactions, helping to develop various types of drugs such as antibacterial, antiviral and anti-tumor.

In the field of materials science, it also plays an important role. It can be used to prepare high-performance polymer materials. After appropriate chemical reactions, it can be introduced into the polymer chain to improve the mechanical properties, thermal stability and chemical corrosion resistance of the materials. And in the rubber industry, it is often used as a vulcanization accelerator to accelerate the vulcanization process of rubber and improve the physical properties and durability of rubber products.

Furthermore, in agriculture, benzothiazole-2-thiol can be used to synthesize pesticides. After rational design and modification, it has high selectivity and biological activity against specific pests or pathogens, effectively preventing and controlling crop diseases and insect pests, and ensuring crop yield and quality.

In addition, in the field of analytical chemistry, due to its unique chemical properties, it can be used as an analytical reagent for the detection and quantitative analysis of specific metal ions. By specifically reacting with metal ions, complexes with special spectral properties are generated to achieve sensitive detection of metal ions. From this perspective, benzothiazole-2-thiol has shown important application value in many fields such as medicine, materials, agriculture and analytical chemistry, providing assistance for the development of various fields.

What are the physical properties of Benzothiazole-2-thiol?

Benzothiazole-2-mercaptan is a kind of organic compound. Its physical properties are particularly important, and it is related to its application in various fields.

First of all, its properties, benzothiazole-2-mercaptan at room temperature, mostly show a light yellow to brown crystalline powder, and it has a certain color and shape. This is its intuitive physical appearance, which is initially recognized by people.

Furthermore, when it comes to the melting point, its melting point is between 168-172 ° C. The melting point is the critical temperature at which a substance changes from a solid state to a liquid state. This specific melting point range makes benzothiazole-2-thiol undergo phase transformation in this temperature range during heating, which is also one of its important physical properties, which is related to its heating change and processing conditions.

Solubility is also a key property. Benzothiazole-2-thiol is insoluble in water, and this property is due to the force between its molecular structure and water molecules. However, it is soluble in some organic solvents, such as ethanol and acetone. The dissolution of organic solvents makes benzothiazole-2-thiol in the field of organic synthesis and other fields, and can use organic solvents to realize dispersion, reaction and other operations, expanding its application scope.

In addition, its odor also has characteristics, with a special mercaptan odor. The generation of odor is related to the sulfur-containing groups in its molecules. Although the description of odor is relatively subjective, the special odor is also a representation of the physical properties of the substance, which can help sensory recognition.

In summary, the physical properties of benzothiazole-2-thiol, such as properties, melting point, solubility, odor, etc., are related to each other, and together build its physical properties system, laying the foundation for its application in many fields such as chemical industry, materials, and medicine.

What are the chemical properties of Benzothiazole-2-thiol?

Benzothiazole-2-mercaptan is an organic compound with unique chemical properties. It is a light yellow to brown crystalline powder and has important uses in many fields.

First of all, benzothiazole-2-mercaptan is significantly acidic. Its intramolecular thiol group (-SH) can release protons and exhibit acidic properties. In specific chemical reactions, it can act as an acid catalyst to accelerate the reaction. For example, in some esterification reactions, the addition of benzothiazole-2-mercaptan can increase the reaction rate, and the conditions are mild, which also has a certain regulatory effect on the selectivity of reactants and products.

Secondly, the compound has strong coordination ability. Due to the presence of lone pair electrons on sulfur atoms and nitrogen atoms, it can form stable complexes with a variety of metal ions. It is widely used in the separation, enrichment and analysis and detection of metal ions. Taking the detection of copper ions as an example, benzothiazole-2-thiol can quickly combine with copper ions to generate complexes with specific color or spectral characteristics, thereby enabling sensitive detection of copper ions.

Furthermore, benzothiazole-2-thiol has high reactivity. Its thiol group is easily oxidized to form disulfide and other products. In the rubber industry, it is often used as a vulcanization accelerator, which can speed up the vulcanization process of rubber, improve the degree of crosslinking and physical and mechanical properties of vulcanized rubber, and significantly improve indicators such as hardness and tensile strength. In addition, in the field of organic synthesis, as an important intermediate, it participates in many organic reactions, and can construct various complex compounds containing benzothiazole structures. These compounds have potential application value in pharmaceutical chemistry, materials science and other fields.

In summary, benzothiazole-2-thiol, with its acidity, coordination ability and high reactivity, plays an indispensable role in chemical engineering, analytical testing, materials and medicine, and provides strong chemical support for the development of various fields.

What are Benzothiazole-2-thiol synthesis methods?

There are several common methods for synthesizing benzothiazole-2-thiol.

One is to use o-aminothiophenol and carbon disulfide as raw materials. In a suitable reaction vessel, mix o-aminothiophenol and carbon disulfide in a certain proportion, and add an appropriate amount of basic catalyst, such as potassium hydroxide or sodium hydroxide. Under heating conditions, the two undergo a condensation reaction. During the reaction, the temperature needs to be carefully controlled, usually maintained at a certain range, such as 60-80 degrees Celsius. In this reaction process, the carbonyl group of carbon disulfide interacts with the amino group and mercapto group of o-aminothiophenol gradually, and after complex changes, the final benzothiazole-2-thiol is obtained. After the reaction is completed, the product is purified by conventional separation methods, such as extraction, distillation, etc.

Second, o-halogenated aniline and thiocyanate are used as starting materials. First, the o-halogenated aniline and thiocyanate are placed in a solvent, such as ethanol or acetone. Add a catalyst, such as a copper salt catalyst. Under heating and stirring conditions, the halogen atom reacts with thiocyanate to form an intermediate of o-thiocyanidine. Subsequently, the intermediate is further cyclized in an acidic or basic environment and converted to benzothiazole-2-thiol. During this process, the choice of solvent, the amount of catalyst, and the reaction temperature and time all have a significant impact on the reaction yield and product purity.

Third, react with sodium hydrosulfide with 2-halobenzothiazole. Put 2-halobenzothiazole into the reaction system and add sodium hydrosulfide solution. At appropriate temperature and pressure, the halogen atom is replaced by hydrogen sulfide to obtain benzothiazole-2-thiol. This method is relatively direct, but the acquisition of 2-halobenzothiazole raw materials may be difficult, and the reaction conditions need to be carefully regulated to achieve the desired reaction effect.

Benzothiazole-2-thiol what are the precautions during use

Benzothiazole-2-thiol is an organic compound. During use, the following things should be paid attention to:
First, this substance has certain toxicity and irritation. It may cause irritation to the eyes, skin and respiratory tract, and even affect human health in serious cases. Therefore, when using, appropriate protective measures must be taken. Operators should wear protective clothing, protective gloves and goggles to prevent it from contacting the skin and eyes. If used in poorly ventilated areas, a gas mask should also be worn to avoid inhaling its volatile gas.
Second, benzothiazole-2-thiol is chemically active. It can react chemically with many substances, such as oxidants, acids, bases, etc. Therefore, when storing and using, it must not be mixed or mixed with such substances to prevent dangerous chemical reactions, such as explosions, fires, etc.
Third, the compound may be harmful to the environment. During use, prevent it from leaking into the environment. If a leak unfortunately occurs, emergency measures should be taken immediately to clean up the leak quickly to prevent it from polluting soil, water sources, etc.
Fourth, benzothiazole-2-thiol will produce toxic gases when heated or burned. Therefore, high temperatures and open flames should be avoided during use, and at the same time, it is necessary to ensure that the use environment is well ventilated so that possible harmful gases can be discharged in time. Fifth, after use, the remaining benzothiazole-2-thiol and related waste must be properly disposed of in accordance with regulations and cannot be discarded at will. When following environmental protection requirements, it should be handed over to professional institutions for disposal to prevent pollution to the environment.