Linshang Chemical
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Benzenecarbothioamide, 4-Chloro- (9Ci)
Linshang Chemical
|
HS Code |
694272 |
| Name | Benzenecarbothioamide, 4 - Chloro - (9Ci) |
| Chemical Formula | C7H6ClNS |
| Molar Mass | 171.65 g/mol |
| Appearance | Solid (predicted) |
| Boiling Point | 334.5°C at 760 mmHg (predicted) |
| Melting Point | 176 - 178°C |
| Density | 1.36 g/cm³ (predicted) |
| Solubility In Water | Insoluble |
| Logp | 2.41 (predicted) |
| Flash Point | 156.1°C (predicted) |
As an accredited Benzenecarbothioamide, 4-Chloro- (9Ci) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4 - chloro - benzenecarbothioamide (9CI) in a sealed chemical - grade container. |
| Storage | **Storage of 4 - chloro - benzenecarbothioamide (9CI)** Store 4 - chloro - benzenecarbothioamide in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. It should be stored in a tightly sealed container to prevent moisture absorption and potential degradation. Also, ensure the storage area is out of reach of unauthorized personnel and in accordance with local safety regulations. |
| Shipping | For the chemical "Benzenecarbothioamide, 4 - chloro - (9ci)", shipping must follow strict regulations. It should be properly packaged to prevent leakage, labeled clearly, and transported by carriers licensed for hazardous or chemical goods. |
Competitive Benzenecarbothioamide, 4-Chloro- (9Ci) prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy Benzenecarbothioamide, 4-Chloro- (9Ci) in China?
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Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading Benzenecarbothioamide, 4-Chloro- (9Ci) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of 4-chlorobenzylthioamide (9CI)?
4-Bromobenzylacetylteanidine (9CI) is also an organic compound. The analysis of its chemical structure requires a detailed study of its atomic connection and functional group composition.
In this compound, bromine (Br) atoms are attached to benzyl groups. The benzyl group is the structure of phenylcyclomethylene (-CH ² -). The acetylteanidine part is derived from acetyl (CH < CO >) and aniline (C < H < NH < 2), that is, acetyl substituted for aniline amino (-NH < 3) hydrogen atoms to form an amide bond (-CONH -) structure.
In summary, the chemical structure of 4-bromobenzylacetylteaniline is: with a phenyl ring as the group, one position is connected to methylene, and the methylene is connected to a bromine atom to form a bromobenzyl group; the other position is connected to the acetylteaniline structure, which is connected by an amide bond. In this way, the arrangement and combination of atoms and functional groups form a unique chemical structure of 4-bromobenzylacetylteaniline, which endows it with specific physical and chemical properties and has specific uses and reactivity in organic synthesis and related fields.
In this compound, bromine (Br) atoms are attached to benzyl groups. The benzyl group is the structure of phenylcyclomethylene (-CH ² -). The acetylteanidine part is derived from acetyl (CH < CO >) and aniline (C < H < NH < 2), that is, acetyl substituted for aniline amino (-NH < 3) hydrogen atoms to form an amide bond (-CONH -) structure.
In summary, the chemical structure of 4-bromobenzylacetylteaniline is: with a phenyl ring as the group, one position is connected to methylene, and the methylene is connected to a bromine atom to form a bromobenzyl group; the other position is connected to the acetylteaniline structure, which is connected by an amide bond. In this way, the arrangement and combination of atoms and functional groups form a unique chemical structure of 4-bromobenzylacetylteaniline, which endows it with specific physical and chemical properties and has specific uses and reactivity in organic synthesis and related fields.
What are the physical properties of 4-chlorobenzylthioamide (9CI)?
4-Deuterated lithium benzoate (9CI) is a chemical substance. Its physical properties have various characteristics.
Under normal temperature and pressure, it often takes the shape of a white crystalline powder, which is easy to store and use. It is easy to handle and has high stability in many chemical operations.
When it comes to solubility, it can show certain solubility properties in water. Water is the solvent of all things, and many substances interact with it. 4-Deuterated lithium benzoate can be moderately dissolved in water, which is related to its reaction and application in aqueous solutions. Solubility makes the ions or molecules in it evenly dispersed, which is conducive to participating in various chemical reactions and provides convenience for chemical synthesis, analysis and other operations.
As for the melting point, it is also one of the important physical properties. The substance has a specific melting point value, which reflects the critical temperature of its solid-state and liquid-state transition. When the ambient temperature rises to the melting point, lithium 4-deuterated benzoate gradually melts from the solid state to the liquid state, which has a great impact on its processing, molding and other industrial applications. Only by accurately controlling the melting point can it be used reasonably in production practice to ensure product quality and performance.
Furthermore, its density cannot be ignored. Density represents the mass per unit volume of a substance, and the density of 4-deuterated lithium benzoate determines its accumulation and distribution in a specific space. In a mixed system, the density difference is related to the phenomenon of stratification and dispersion of substances, which is of guiding significance for the mixing and separation of materials in the chemical production process.
This is a summary of the physical properties of 4-deuterated lithium benzoate (9CI). Each property is interrelated and together determines its behavior and use in the chemical field.
Under normal temperature and pressure, it often takes the shape of a white crystalline powder, which is easy to store and use. It is easy to handle and has high stability in many chemical operations.
When it comes to solubility, it can show certain solubility properties in water. Water is the solvent of all things, and many substances interact with it. 4-Deuterated lithium benzoate can be moderately dissolved in water, which is related to its reaction and application in aqueous solutions. Solubility makes the ions or molecules in it evenly dispersed, which is conducive to participating in various chemical reactions and provides convenience for chemical synthesis, analysis and other operations.
As for the melting point, it is also one of the important physical properties. The substance has a specific melting point value, which reflects the critical temperature of its solid-state and liquid-state transition. When the ambient temperature rises to the melting point, lithium 4-deuterated benzoate gradually melts from the solid state to the liquid state, which has a great impact on its processing, molding and other industrial applications. Only by accurately controlling the melting point can it be used reasonably in production practice to ensure product quality and performance.
Furthermore, its density cannot be ignored. Density represents the mass per unit volume of a substance, and the density of 4-deuterated lithium benzoate determines its accumulation and distribution in a specific space. In a mixed system, the density difference is related to the phenomenon of stratification and dispersion of substances, which is of guiding significance for the mixing and separation of materials in the chemical production process.
This is a summary of the physical properties of 4-deuterated lithium benzoate (9CI). Each property is interrelated and together determines its behavior and use in the chemical field.
What are the common uses of 4-chlorobenzylthioamide (9CI)?
Methyl 4-% cyanophenylacetate (9CI) is often used in many delicate formulas for its unique properties. This drug is often a key material in the process of synthesis. In the art of organic synthesis, it often appears in the process of building complex carbon frames. The cover contains cyanobenzene and ester groups because of its structure, both of which are active and can trigger a variety of reactions.
In the past, organic synthesizers often came into contact with nucleophiles. Cyanobenzene can be converted into ring-opening cyanobenzene groups, and ester groups can also be hydrolyzed, alcoholyzed or aminolyzed, resulting in a variety of compounds. It is also very popular in the way of pharmaceutical creation. Based on it, molecules with specific pharmacological activities can be derived, either as antibacterial agents or as analgesic drugs, to help the healing industry.
And in the art of fragrance preparation, it can be skillfully transformed to produce a unique aroma substance, which adds color to the fragrance. When the craftsman operates, he must pay attention to the temperature of the reaction, the ratio of time and agent, in order to obtain exquisite results. Because of its cyanide group toxicity, it must be strictly followed when used to prevent problems before they occur. In short, 4-% cyanophenylacetate methyl ester (9CI) has its indispensable position in the chemical, pharmaceutical, and fragrance industries, and has made great contributions to the advancement of various skills.
In the past, organic synthesizers often came into contact with nucleophiles. Cyanobenzene can be converted into ring-opening cyanobenzene groups, and ester groups can also be hydrolyzed, alcoholyzed or aminolyzed, resulting in a variety of compounds. It is also very popular in the way of pharmaceutical creation. Based on it, molecules with specific pharmacological activities can be derived, either as antibacterial agents or as analgesic drugs, to help the healing industry.
And in the art of fragrance preparation, it can be skillfully transformed to produce a unique aroma substance, which adds color to the fragrance. When the craftsman operates, he must pay attention to the temperature of the reaction, the ratio of time and agent, in order to obtain exquisite results. Because of its cyanide group toxicity, it must be strictly followed when used to prevent problems before they occur. In short, 4-% cyanophenylacetate methyl ester (9CI) has its indispensable position in the chemical, pharmaceutical, and fragrance industries, and has made great contributions to the advancement of various skills.
What are the synthesis methods of 4-chlorobenzylthioamide (9CI)?
The synthesis of methyl 4-cyanothiophene acetate (9CI) is an important topic in organic synthesis. There are several common methods for its synthesis.
One is to use thiophene as the starting material. First, thiophene is brominated under specific conditions, and bromine atoms are introduced to generate bromothiophene. This bromothiophene interacts with cyanide reagents, and through nucleophilic substitution, the bromine atoms are replaced by cyanyl groups to obtain cyanothiophene. After cyanothiophene and reagents containing methyl ester groups, under suitable catalyst and reaction conditions, through a series of reactions, methyl 4-cyanothiophene acetate can be obtained. For example, a metal catalyst can be used to catalyze the nucleophilic substitution of cyanothiophene with methyl haloacetate to achieve the synthesis of the target product.
The second method can start from the carboxylic acid derivative containing the thiophene ring. The carboxylic acid is first converted into the corresponding acid chloride, and then reacted with the reagent containing the cyanoyl group and the methyl ester group. This reaction may involve the nucleophilic addition-elimination mechanism. The carbonyl group of the acid chloride reacts with the nucleophilic reagent. After the intermediate product is converted, the final product is methyl 4-cyanothiophene acetate. In this process, the control of reaction conditions is crucial, such as temperature and solvent selection, which all affect the yield and selectivity of the reaction.
Another synthetic path is to take a specific heterocyclic compound as the starting material and undergo multi-step functional group transformation. For example, through cyclization, cyano introduction, methyl esterification and other steps, the molecular structure of methyl 4-cyanothiophene acetate is gradually constructed. This path requires fine regulation of the reaction conditions of each step, and attention should be paid to the interaction between functional groups to avoid unnecessary side reactions and improve the purity and yield of the target product.
One is to use thiophene as the starting material. First, thiophene is brominated under specific conditions, and bromine atoms are introduced to generate bromothiophene. This bromothiophene interacts with cyanide reagents, and through nucleophilic substitution, the bromine atoms are replaced by cyanyl groups to obtain cyanothiophene. After cyanothiophene and reagents containing methyl ester groups, under suitable catalyst and reaction conditions, through a series of reactions, methyl 4-cyanothiophene acetate can be obtained. For example, a metal catalyst can be used to catalyze the nucleophilic substitution of cyanothiophene with methyl haloacetate to achieve the synthesis of the target product.
The second method can start from the carboxylic acid derivative containing the thiophene ring. The carboxylic acid is first converted into the corresponding acid chloride, and then reacted with the reagent containing the cyanoyl group and the methyl ester group. This reaction may involve the nucleophilic addition-elimination mechanism. The carbonyl group of the acid chloride reacts with the nucleophilic reagent. After the intermediate product is converted, the final product is methyl 4-cyanothiophene acetate. In this process, the control of reaction conditions is crucial, such as temperature and solvent selection, which all affect the yield and selectivity of the reaction.
Another synthetic path is to take a specific heterocyclic compound as the starting material and undergo multi-step functional group transformation. For example, through cyclization, cyano introduction, methyl esterification and other steps, the molecular structure of methyl 4-cyanothiophene acetate is gradually constructed. This path requires fine regulation of the reaction conditions of each step, and attention should be paid to the interaction between functional groups to avoid unnecessary side reactions and improve the purity and yield of the target product.
What are the precautions for the use of 4-chlorobenzylthioamide (9CI)?
4-% fluoroacetic acid (9CI), there are things to be paid attention to when using it. This product is toxic, and it must be used in accordance with the product instructions and the instructions of the user. Do not make decisions without authorization, and change the method or amount of use without authorization.
Furthermore, store it properly. It should be placed in the environment, dry and children can't reach it, so as to prevent children from eating and becoming big. And to avoid fire and source, so as not to change the quality, affect the effectiveness, and even cause danger.
When using the product, also do a good job of prevention. If you wear gloves, masks, etc., avoid direct contact with the skin and respiratory tract. If you accidentally contact the product, whether it is contaminated with the skin or inhaled, you should take immediate measures. If the skin is connected, wash it with a lot of water as soon as possible; if it is absorbed, it should be rushed to a well-connected place. If necessary, it should be treated immediately.
Same, after use, the remaining products should not be used up, and they should be properly handled according to the relevant regulations to prevent contamination of the environment, and others. In addition, those who use this product should be careful to ensure safety.
Furthermore, store it properly. It should be placed in the environment, dry and children can't reach it, so as to prevent children from eating and becoming big. And to avoid fire and source, so as not to change the quality, affect the effectiveness, and even cause danger.
When using the product, also do a good job of prevention. If you wear gloves, masks, etc., avoid direct contact with the skin and respiratory tract. If you accidentally contact the product, whether it is contaminated with the skin or inhaled, you should take immediate measures. If the skin is connected, wash it with a lot of water as soon as possible; if it is absorbed, it should be rushed to a well-connected place. If necessary, it should be treated immediately.
Same, after use, the remaining products should not be used up, and they should be properly handled according to the relevant regulations to prevent contamination of the environment, and others. In addition, those who use this product should be careful to ensure safety.
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