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N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate
Linshang Chemical
|
HS Code |
731534 |
| Chemical Name | N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate |
As an accredited N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of N - ethylethanamine 2 - [(2,6 - dichlorophenyl)amino]benzeneacetate in sealed plastic bags. |
| Storage | Store N - ethylethanamine 2 - [(2,6 - dichlorophenyl)amino]benzeneacetate in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent moisture absorption and degradation. This compound should be stored separately from incompatible substances to avoid potential reactions. |
| Shipping | N - ethylethanamine 2 - [(2,6 - dichlorophenyl)amino]benzeneacetate is shipped in specialized, well - sealed containers. Strict adherence to chemical transportation regulations ensures safe transit, avoiding exposure and maintaining product integrity. |
Competitive N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate prices that fit your budget—flexible terms and customized quotes for every order.
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Where to Buy N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate in China?
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As a leading N-Ethylethanamine 2-[(2,6-Dichlorophenyl)Amino]Benzeneacetate 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 N-ethylethanamine 2- [ (2,6-dichlorophenyl) amino] benzeneacetate
Alas! The synthesis of these two substances needs to be investigated. For N-ethylethanamine, ethylene diethylamine is also of the formula C-H-N. With an amino group, it is diethyl with a nitrogen atom.
And 2 - [ (2,6-dichlorophenyl) amino] phenylacetic acid is slightly more complex. On the benzene of phenylacetic acid, the group is connected to the [ (2,6-dichlorophenyl) amino] in the binary position. In this group, the chlorine atom of 2,6-dichlorophenyl is located at the second and sixth positions of benzene, and it is related to the benzene of amino-phenylacetic acid. As for acetic acid, it is formed by the reaction of acetic acid.
For example, N-ethylethanamine and 2-[ (2,6-dichlorophenyl) amino] phenylacetic acid contain polyatoms, carboxyl groups, etc., and their properties and uses may vary depending on their properties.
And 2 - [ (2,6-dichlorophenyl) amino] phenylacetic acid is slightly more complex. On the benzene of phenylacetic acid, the group is connected to the [ (2,6-dichlorophenyl) amino] in the binary position. In this group, the chlorine atom of 2,6-dichlorophenyl is located at the second and sixth positions of benzene, and it is related to the benzene of amino-phenylacetic acid. As for acetic acid, it is formed by the reaction of acetic acid.
For example, N-ethylethanamine and 2-[ (2,6-dichlorophenyl) amino] phenylacetic acid contain polyatoms, carboxyl groups, etc., and their properties and uses may vary depending on their properties.
What are the main uses of N-ethylethanamine 2- [ (2,6-dichlorophenyl) amino] benzeneacetate
The composition of N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetate has a wide range of uses.
First, in the field of medicine, it can be used as an active ingredient for the development of new drugs. The combination of the chemical properties of the two may exhibit unique pharmacological activities, which can be helpful for the treatment of specific diseases. For example, it can interact with human biomolecules through its special structure for certain inflammatory or nervous system diseases, or can regulate physiological functions, relieve symptoms, and even cure diseases.
Second, in organic synthetic chemistry, it can be a key intermediate. Organic synthesis aims to create complex organic molecules. With its specific functional groups, this compound can participate in various chemical reactions, such as nucleophilic substitution, addition reactions, etc. By ingeniously designing reaction routes and using it as a starting material, many organic compounds with novel structures can be derived, expanding new directions for organic chemistry research and enriching the variety of compounds.
Third, in the field of materials science, it may have potential application value. With the development of materials science, the demand for materials with special properties is increasing. The compound may endow the material with certain special properties due to its structural characteristics, such as improving the stability and solubility of the material, or endowing the material with optical and electrical properties. For example, in the preparation of new polymer materials, the addition of this compound may optimize the material properties and meet the needs of different engineering applications.
First, in the field of medicine, it can be used as an active ingredient for the development of new drugs. The combination of the chemical properties of the two may exhibit unique pharmacological activities, which can be helpful for the treatment of specific diseases. For example, it can interact with human biomolecules through its special structure for certain inflammatory or nervous system diseases, or can regulate physiological functions, relieve symptoms, and even cure diseases.
Second, in organic synthetic chemistry, it can be a key intermediate. Organic synthesis aims to create complex organic molecules. With its specific functional groups, this compound can participate in various chemical reactions, such as nucleophilic substitution, addition reactions, etc. By ingeniously designing reaction routes and using it as a starting material, many organic compounds with novel structures can be derived, expanding new directions for organic chemistry research and enriching the variety of compounds.
Third, in the field of materials science, it may have potential application value. With the development of materials science, the demand for materials with special properties is increasing. The compound may endow the material with certain special properties due to its structural characteristics, such as improving the stability and solubility of the material, or endowing the material with optical and electrical properties. For example, in the preparation of new polymer materials, the addition of this compound may optimize the material properties and meet the needs of different engineering applications.
What are the physical properties of N-ethylethanamine 2- [ (2,6-dichlorophenyl) amino] benzeneacetate
N-ethylethanamine (N-ethylethylamine) is an organic base. It is a colorless liquid at room temperature and has an ammonia taste. It can form salts with acids and is often used as a base reagent or intermediate in organic synthesis. It is alkaline and can neutralize with acids to form corresponding salts.
2 - [ (2,6-dichlorophenyl) amino] benzeneacetate (2 - [ (2,6-dichlorophenyl) amino] phenylacetate), which is a phenylacetic acid derivative containing a specific substituent. Because it contains groups such as benzene ring, chlorine atom and amino group, it may have certain lipid solubility and specific chemical activity. From a structural point of view, the benzene ring imparts a certain stability and conjugation effect. The electronegativity of the chlorine atom may affect the polarity and reactivity of the molecule. The amino group can participate in a variety of chemical reactions, such as nucleophilic substitution. The structural part of phenylacetate may have a certain binding ability with metal ions.
When both coexist, the alkalinity of N-ethylethanamine or the acidic group of 2 - [ (2,6 - dichlorophenyl) amino] benzeneacetate (if ionizable hydrogen is present) reacts to form corresponding salt compounds and changes the original physical properties. The resulting salt is different in solubility or from the original compound, and its solubility or decrease in organic solvents, and its solubility in water or increases due to the ionic characteristics of the salt. From the perspective of melting point and boiling point, after the formation of salt, the intermolecular force changes, or the melting point and boiling point change. And because of the existence of diverse groups in the structure of the two, or the mixture presents a unique absorption peak in spectral properties, etc., it can be used as a basis for analysis and identification.
2 - [ (2,6-dichlorophenyl) amino] benzeneacetate (2 - [ (2,6-dichlorophenyl) amino] phenylacetate), which is a phenylacetic acid derivative containing a specific substituent. Because it contains groups such as benzene ring, chlorine atom and amino group, it may have certain lipid solubility and specific chemical activity. From a structural point of view, the benzene ring imparts a certain stability and conjugation effect. The electronegativity of the chlorine atom may affect the polarity and reactivity of the molecule. The amino group can participate in a variety of chemical reactions, such as nucleophilic substitution. The structural part of phenylacetate may have a certain binding ability with metal ions.
When both coexist, the alkalinity of N-ethylethanamine or the acidic group of 2 - [ (2,6 - dichlorophenyl) amino] benzeneacetate (if ionizable hydrogen is present) reacts to form corresponding salt compounds and changes the original physical properties. The resulting salt is different in solubility or from the original compound, and its solubility or decrease in organic solvents, and its solubility in water or increases due to the ionic characteristics of the salt. From the perspective of melting point and boiling point, after the formation of salt, the intermolecular force changes, or the melting point and boiling point change. And because of the existence of diverse groups in the structure of the two, or the mixture presents a unique absorption peak in spectral properties, etc., it can be used as a basis for analysis and identification.
What is the preparation method of N-ethylethanamine 2- [ (2,6-dichlorophenyl) amino] benzeneacetate
To prepare N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetate, the method is as follows:
Prepare all the necessary things, such as suitable raw materials and utensils. In a clean vessel, take an appropriate amount of N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetic acid with accurate measurement. The amount of these two should be determined according to the amount of the product prepared and the reason of the reaction.
Then, place the two slowly in the reaction vessel, and at the same time, pay attention to the surrounding temperature and humidity. The two can react smoothly at a specific temperature and humidity. If the temperature is too high or too low, it can cause the reaction to deviate.
It can be used as a stirring device to make the two uniform and accelerate the process of the reaction. And when the reaction is completed, it is necessary to monitor its changes at all times, or observe the change of its color, or observe the change of its texture.
After the reaction is completed, the product can be properly separated. Or by filtration, the solid-liquid separation; or by distillation, according to the boiling point, the product of pure 2 - [ (2,6 - dichlorophenyl) amino] phenylacetate and N - ethylethylamine is obtained.
Then by washing, remove its impurities, and then dry it to obtain pure N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetate. The whole process must be carefully handled, and a little carelessness will cause the product to be impure and not meet the needs.
Prepare all the necessary things, such as suitable raw materials and utensils. In a clean vessel, take an appropriate amount of N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetic acid with accurate measurement. The amount of these two should be determined according to the amount of the product prepared and the reason of the reaction.
Then, place the two slowly in the reaction vessel, and at the same time, pay attention to the surrounding temperature and humidity. The two can react smoothly at a specific temperature and humidity. If the temperature is too high or too low, it can cause the reaction to deviate.
It can be used as a stirring device to make the two uniform and accelerate the process of the reaction. And when the reaction is completed, it is necessary to monitor its changes at all times, or observe the change of its color, or observe the change of its texture.
After the reaction is completed, the product can be properly separated. Or by filtration, the solid-liquid separation; or by distillation, according to the boiling point, the product of pure 2 - [ (2,6 - dichlorophenyl) amino] phenylacetate and N - ethylethylamine is obtained.
Then by washing, remove its impurities, and then dry it to obtain pure N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetate. The whole process must be carefully handled, and a little carelessness will cause the product to be impure and not meet the needs.
N-ethylethanamine 2- [ (2,6-dichlorophenyl) amino] benzeneacetate
When applying N-ethylethylamine and 2- [ (2,6-dichlorophenyl) amino] phenylacetate, many matters must be paid attention to.
First, both are chemical substances with certain chemical activity and latent risk. During operation, it is necessary to wear appropriate protective equipment, such as gloves, goggles, protective clothing, etc., to prevent direct contact of chemicals with skin, eyes, etc., causing physical damage.
Second, the reaction process may involve specific conditions, such as temperature, pressure, reaction time and the use of catalysts. Precise control of these conditions is essential, and a slight deviation may affect the reaction process and product quality. If the temperature is too high, or the reaction rate is too fast, causing an increase in side reactions; if the temperature is too low, the reaction will be slow and may not even occur.
Third, the chemical substances involved in the reaction of the two may be toxic, corrosive or volatile. Therefore, the operation should be placed in a well-ventilated place, such as a fume hood, to avoid the accumulation of harmful gases and endanger the health of the operator. And the waste generated by the reaction should be properly disposed of according to regulations and should not be discarded at will, so as not to pollute the environment.
Fourth, when taking and mixing the two, the operating procedures should be strictly followed and carried out in exact proportions. Dosage errors or incomplete reactions, or the formation of unexpected products.
Fifth, the reaction process should be closely observed, such as color changes, gas generation, precipitation, etc., in order to detect abnormalities in time and take appropriate measures.
In short, when using these two, strictly follow relevant procedures and safety guidelines to ensure safe and efficient operation and achieve the desired reaction effect.
First, both are chemical substances with certain chemical activity and latent risk. During operation, it is necessary to wear appropriate protective equipment, such as gloves, goggles, protective clothing, etc., to prevent direct contact of chemicals with skin, eyes, etc., causing physical damage.
Second, the reaction process may involve specific conditions, such as temperature, pressure, reaction time and the use of catalysts. Precise control of these conditions is essential, and a slight deviation may affect the reaction process and product quality. If the temperature is too high, or the reaction rate is too fast, causing an increase in side reactions; if the temperature is too low, the reaction will be slow and may not even occur.
Third, the chemical substances involved in the reaction of the two may be toxic, corrosive or volatile. Therefore, the operation should be placed in a well-ventilated place, such as a fume hood, to avoid the accumulation of harmful gases and endanger the health of the operator. And the waste generated by the reaction should be properly disposed of according to regulations and should not be discarded at will, so as not to pollute the environment.
Fourth, when taking and mixing the two, the operating procedures should be strictly followed and carried out in exact proportions. Dosage errors or incomplete reactions, or the formation of unexpected products.
Fifth, the reaction process should be closely observed, such as color changes, gas generation, precipitation, etc., in order to detect abnormalities in time and take appropriate measures.
In short, when using these two, strictly follow relevant procedures and safety guidelines to ensure safe and efficient operation and achieve the desired reaction effect.
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