Linshang Chemical
PRODUCTS
Benzenemethanamine, 2-Chloro-3-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
953695 |
| Chemical Formula | C8H7ClF3N |
| Molar Mass | 211.596 g/mol |
As an accredited Benzenemethanamine, 2-Chloro-3-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottle packaging for 2 - chloro - 3 - (trifluoromethyl)benzenemethanamine. |
| Storage | Store "2 - chloro - 3 - (trifluoromethyl)benzenemethanamine" in a cool, dry, well - ventilated area. Keep it away from heat, open flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant materials. This helps prevent decomposition, evaporation, and potential reactions that could pose safety risks. |
| Shipping | Benzenemethanamine, 2 - chloro - 3 - (trifluoromethyl)- is shipped in accordance with strict chemical regulations. Packed in specialized containers, it's transported by approved carriers to ensure safety during transit. |
Competitive Benzenemethanamine, 2-Chloro-3-(Trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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What is the chemical structure of this product "2-chloro-3- (trifluoromethyl) aniline"?
"The chemical structure of this product, '2-hydrogen-3- (triethylmethyl) thioacetamide', is involved in the field of organic chemistry. Looking at its name, '2-hydrogen' indicates that there is a hydrogen atom occupying a specific position in the molecular structure; '3- (triethylmethyl) ' indicates that there is a triethyl group connected at the third position. This group is composed of three ethyl groups and a methyl group. Ethyl is the remaining part after ethane removes a hydrogen atom, and methyl is methane removes a hydrogen atom. As for "thioacetamide", the word "thio" suggests that the structure contains a sulfur heterocycle, which is commonly used as a variant of the thiophene ring. "Acetamide" means that there is an acetamide structure, and the acetyl group is the rest of the acetic acid after removing the hydroxyl group, which is connected to the amino group.
Therefore, the chemical structure of this compound is roughly as follows: the sulfur heterocycle is the core structure, there is a hydrogen atom at the second position, and the third position is connected to a triethyl group composed of three ethyl groups and one methyl group, and contains an acetamide structure. This structure endows the compound with specific physical and chemical properties, and may have unique uses and reactivity in organic synthesis, drug research and development, etc. Due to the interaction of various groups in the structure, it can show special chemical behavior and potential application value. "
Therefore, the chemical structure of this compound is roughly as follows: the sulfur heterocycle is the core structure, there is a hydrogen atom at the second position, and the third position is connected to a triethyl group composed of three ethyl groups and one methyl group, and contains an acetamide structure. This structure endows the compound with specific physical and chemical properties, and may have unique uses and reactivity in organic synthesis, drug research and development, etc. Due to the interaction of various groups in the structure, it can show special chemical behavior and potential application value. "
What are the physical properties of "2-chloro-3- (trifluoromethyl) aniline"?
"2-Chloro-3- (triethylmethyl) pyridyl aldehyde" is one of the organic compounds. Its physical properties are quite unique. At room temperature, it is mostly in a liquid state. It may have a certain color or be clear and transparent. Its smell may be irritating, but the exact taste needs to be smelled by yourself in order to accurately perceive it.
As for its melting point, the melting point is due to the interaction of chlorine atoms with pyridine rings and alkyl groups in the structure, resulting in different intermolecular forces. After experimental testing, or in a specific low temperature range, it gradually melts from a solid state to a liquid state. The boiling point changes from a liquid state to a gas state due to the combined effect of intermolecular forces, or at a relatively high temperature.
In terms of solubility, because it contains polar chlorine atoms and pyridine rings, it may have a certain solubility in polar solvents such as alcohols; while in non-polar solvents such as alkanes, the solubility may be relatively small. This is due to the principle of "similar miscibility", polar substances are easily soluble in polar solvents, and non-polar substances are easily soluble in non-polar solvents.
Density above, compared with common water, may be different. Due to the type, number and arrangement of atoms in the molecule, its mass per unit volume is different from water. Either heavier than water or lighter than water can be determined by accurate density measurement experiments.
To sum up, the physical properties of "2-chloro-3- (triethyl) pyridyl aldehyde" are determined by its molecular structure, and exhibit specific behaviors in terms of melting point, boiling point, solubility, density, etc.
As for its melting point, the melting point is due to the interaction of chlorine atoms with pyridine rings and alkyl groups in the structure, resulting in different intermolecular forces. After experimental testing, or in a specific low temperature range, it gradually melts from a solid state to a liquid state. The boiling point changes from a liquid state to a gas state due to the combined effect of intermolecular forces, or at a relatively high temperature.
In terms of solubility, because it contains polar chlorine atoms and pyridine rings, it may have a certain solubility in polar solvents such as alcohols; while in non-polar solvents such as alkanes, the solubility may be relatively small. This is due to the principle of "similar miscibility", polar substances are easily soluble in polar solvents, and non-polar substances are easily soluble in non-polar solvents.
Density above, compared with common water, may be different. Due to the type, number and arrangement of atoms in the molecule, its mass per unit volume is different from water. Either heavier than water or lighter than water can be determined by accurate density measurement experiments.
To sum up, the physical properties of "2-chloro-3- (triethyl) pyridyl aldehyde" are determined by its molecular structure, and exhibit specific behaviors in terms of melting point, boiling point, solubility, density, etc.
What are the applications of "2-chloro-3- (trifluoromethyl) aniline"?
"2-Cyanogen-3- (trifluoromethyl) pyridine" has its uses in the fields of medicine, manufacturing, agriculture and planting.
In the field of medicine, it is a key raw material for the creation of medicine. It can be used to make antibacterial drugs, inhibit the growth of bacteria, heal diseases, and treat diseases and diseases for all living beings. In the research and development of antiviral drugs, it also has its merits, helping doctors find ways to control viruses and protect the health of all people.
In the world of engineering, it is quite useful in material creation. It can be integrated into the system of special plastics to make plastic products optimized, increase their corrosion resistance and weather resistance, and is widely used in chemical equipment and outdoor facilities. In the manufacture of electronic materials, it is also indispensable, helping to form electronic components with excellent performance, making electronic devices more delicate and efficient.
In the context of agriculture and planting, it is an important component in the creation of pesticides. It can produce high-efficiency insecticides, accurately eliminate pests, protect crops from pests, and ensure a bumper harvest. In the research and development of herbicides, it can also be used to remove weeds, help crops thrive, and ensure the abundance of agricultural products.
"2-Cyano-3- (trifluoromethyl) pyridine" is widely used and is key in many fields. It has far-reaching impact on people's livelihood and the progress of science and technology.
In the field of medicine, it is a key raw material for the creation of medicine. It can be used to make antibacterial drugs, inhibit the growth of bacteria, heal diseases, and treat diseases and diseases for all living beings. In the research and development of antiviral drugs, it also has its merits, helping doctors find ways to control viruses and protect the health of all people.
In the world of engineering, it is quite useful in material creation. It can be integrated into the system of special plastics to make plastic products optimized, increase their corrosion resistance and weather resistance, and is widely used in chemical equipment and outdoor facilities. In the manufacture of electronic materials, it is also indispensable, helping to form electronic components with excellent performance, making electronic devices more delicate and efficient.
In the context of agriculture and planting, it is an important component in the creation of pesticides. It can produce high-efficiency insecticides, accurately eliminate pests, protect crops from pests, and ensure a bumper harvest. In the research and development of herbicides, it can also be used to remove weeds, help crops thrive, and ensure the abundance of agricultural products.
"2-Cyano-3- (trifluoromethyl) pyridine" is widely used and is key in many fields. It has far-reaching impact on people's livelihood and the progress of science and technology.
What are the methods for preparing "2-chloro-3- (trifluoromethyl) aniline"?
The preparation method of "2-deuterium-3- (triethylmethyl) furanacetic acid" is not detailed in the classic "Tiangong Kaiwu", but it can be deduced according to the wisdom of the ancients and related chemical process ideas.
First, raw material selection and preparation. To make this product, when looking for suitable raw materials containing deuterium, deuterium is commonly found in heavy water, and deuterium sources can be obtained from heavy water. As for triethylmethyl-related raw materials, or obtained from corresponding hydrocarbons through a series of reactions, hydrocarbons can be obtained from natural oil, coal and other basic hydrocarbons that can be simulated by ancient methods such as fractionation and cracking, and then introduced and converted into functional groups. The basic furan ring of furanacetic acid can be prepared from natural products containing furan structure or by organic synthesis, starting with common organic raw materials such as furfural.
Second, the reaction step. The deuterium-containing raw materials can be reacted with appropriate reagents first to introduce deuterium atoms to suitable positions. In this step, attention should be paid to the mildness of the reaction conditions to ensure the precise integration of deuterium atoms and not affect other subsequent reaction check points. Then, the deuterium-containing part is connected to the triethylmethyl raw materials through condensation, substitution and other reactions. This process may require the help of catalysts. Although the ancients did not have the concept of modern precise catalysts, they could find natural minerals, acids and bases and other substances to promote the reaction. When the structure containing deuterium and triethylmethyl is constructed, it is esterified and substituted with the related precursors of furanacetic acid to form the target "2-deuterium-3- (triethylmethyl) furanacetic acid". In the reaction, it is necessary to strictly control the temperature, time, material ratio and other factors, and the temperature is controlled or controlled according to the temperature. For example, it is adjusted by different temperatures such as slow fire and martial fire. The time is determined according to experience and observation of reaction phenomena. Although the proportion of materials is not accurately measured, it can be explored according to the approximate ratio, and the reaction is sufficient and the product is pure.
Third, the product is separated and purified. After the reaction, the product is mixed in the reaction system and can be separated according to its physical properties and impurities. If the solubility is different, choose a suitable solvent, use the method of recrystallization, and crystallize many times to improve the purity. Or use the difference in boiling point, use the technique of distillation, control the appropriate temperature, and collect the target product fraction. After these steps, a relatively pure "2-deuterium-3- (triethylmethyl) furanacetic acid" can be obtained.
First, raw material selection and preparation. To make this product, when looking for suitable raw materials containing deuterium, deuterium is commonly found in heavy water, and deuterium sources can be obtained from heavy water. As for triethylmethyl-related raw materials, or obtained from corresponding hydrocarbons through a series of reactions, hydrocarbons can be obtained from natural oil, coal and other basic hydrocarbons that can be simulated by ancient methods such as fractionation and cracking, and then introduced and converted into functional groups. The basic furan ring of furanacetic acid can be prepared from natural products containing furan structure or by organic synthesis, starting with common organic raw materials such as furfural.
Second, the reaction step. The deuterium-containing raw materials can be reacted with appropriate reagents first to introduce deuterium atoms to suitable positions. In this step, attention should be paid to the mildness of the reaction conditions to ensure the precise integration of deuterium atoms and not affect other subsequent reaction check points. Then, the deuterium-containing part is connected to the triethylmethyl raw materials through condensation, substitution and other reactions. This process may require the help of catalysts. Although the ancients did not have the concept of modern precise catalysts, they could find natural minerals, acids and bases and other substances to promote the reaction. When the structure containing deuterium and triethylmethyl is constructed, it is esterified and substituted with the related precursors of furanacetic acid to form the target "2-deuterium-3- (triethylmethyl) furanacetic acid". In the reaction, it is necessary to strictly control the temperature, time, material ratio and other factors, and the temperature is controlled or controlled according to the temperature. For example, it is adjusted by different temperatures such as slow fire and martial fire. The time is determined according to experience and observation of reaction phenomena. Although the proportion of materials is not accurately measured, it can be explored according to the approximate ratio, and the reaction is sufficient and the product is pure.
Third, the product is separated and purified. After the reaction, the product is mixed in the reaction system and can be separated according to its physical properties and impurities. If the solubility is different, choose a suitable solvent, use the method of recrystallization, and crystallize many times to improve the purity. Or use the difference in boiling point, use the technique of distillation, control the appropriate temperature, and collect the target product fraction. After these steps, a relatively pure "2-deuterium-3- (triethylmethyl) furanacetic acid" can be obtained.
What is the market outlook for "2-chloro-3- (trifluoromethyl) aniline"?
In today's world, the prospects of "2-halogen-3 - (triethylmethyl) thiaacetamide" in the market are related to many parties and are worth exploring.
Looking at the field of medicine, this substance may have a unique pharmacology. Today's diseases are diverse, and medical needs are vast. If it emerges in pharmacological research, it has a significant effect on specific diseases. If it can act on the pathological link of certain intractable diseases, it may open up new treatment methods. With the current development trend of medicine, innovative drugs are highly sought after. If "2-halo-3- (triethylmethyl) thioacetamide" can pass rigorous clinical trials and prove its safety and effectiveness, it will be able to win a place in the pharmaceutical market, bring good news to many patients, and create huge profits for pharmaceutical companies.
In the chemical industry, this compound may be a key intermediate. The chemical production chain is interconnected, and the demand for intermediates is stable and large. If "2-halo-3- (triethylmethyl) thioacetamide" can show efficient and stable characteristics in the chemical synthesis process, as a key link between the previous and the next, it can promote the production of a series of downstream products. From new materials to fine chemicals, it is possible to gain innovative development opportunities. Its market size may grow steadily with the expansion of the chemical industry.
However, although the market prospect has potential, there are also challenges. R & D costs are high, from laboratory synthesis to industrial production, many links require a lot of capital and manpower investment. Regulations and regulations are increasingly stringent, and many quality and safety standards need to be met. And the market competition is fierce, and similar or alternative products may have occupied part of the share. Only by continuously improving technology, reducing costs, strictly abiding by regulations, and strengthening quality can we break through the market wave and make the market prospect of "2-halogen-3 - (triethyl) thioacetamide" from possible to reality and shine.
Looking at the field of medicine, this substance may have a unique pharmacology. Today's diseases are diverse, and medical needs are vast. If it emerges in pharmacological research, it has a significant effect on specific diseases. If it can act on the pathological link of certain intractable diseases, it may open up new treatment methods. With the current development trend of medicine, innovative drugs are highly sought after. If "2-halo-3- (triethylmethyl) thioacetamide" can pass rigorous clinical trials and prove its safety and effectiveness, it will be able to win a place in the pharmaceutical market, bring good news to many patients, and create huge profits for pharmaceutical companies.
In the chemical industry, this compound may be a key intermediate. The chemical production chain is interconnected, and the demand for intermediates is stable and large. If "2-halo-3- (triethylmethyl) thioacetamide" can show efficient and stable characteristics in the chemical synthesis process, as a key link between the previous and the next, it can promote the production of a series of downstream products. From new materials to fine chemicals, it is possible to gain innovative development opportunities. Its market size may grow steadily with the expansion of the chemical industry.
However, although the market prospect has potential, there are also challenges. R & D costs are high, from laboratory synthesis to industrial production, many links require a lot of capital and manpower investment. Regulations and regulations are increasingly stringent, and many quality and safety standards need to be met. And the market competition is fierce, and similar or alternative products may have occupied part of the share. Only by continuously improving technology, reducing costs, strictly abiding by regulations, and strengthening quality can we break through the market wave and make the market prospect of "2-halogen-3 - (triethyl) thioacetamide" from possible to reality and shine.
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