Linshang Chemical
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2-((2,6-Dichlorophenyl)Amino)-Benzeneacetic Aci Carboxymethyl Ester
Linshang Chemical
|
HS Code |
793536 |
| Chemical Formula | C15H12Cl2NO2 |
| Molar Mass | 308.17 g/mol |
As an accredited 2-((2,6-Dichlorophenyl)Amino)-Benzeneacetic Aci Carboxymethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-((2,6 - dichlorophenyl)amino) - benzeneacetic Aci Carboxymethyl Ester in sealed plastic bags. |
| Storage | Store 2-((2,6 - dichlorophenyl)amino)-benzeneacetic Aci Carboxymethyl Ester in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and exposure to air. Store it separately from incompatible substances, such as strong oxidizers and bases, to avoid potential reactions. |
| Shipping | The chemical 2-((2,6 - dichlorophenyl)amino)-benzeneacetic Aci Carboxymethyl Ester should be shipped in well - sealed, corrosion - resistant containers. Ensure proper labeling indicating its hazardous nature, and follow all relevant regulations for chemical transport. |
Competitive 2-((2,6-Dichlorophenyl)Amino)-Benzeneacetic Aci Carboxymethyl Ester prices that fit your budget—flexible terms and customized quotes for every order.
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What are the chemical properties of 2- ((2,6-dichlorophenyl) amino) -phenylacetate carboxymethyl ester
2-%28%282%2C6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29-%E8%8B%AF%E4%B9%99%E9%85%B8%E7%BE%A7%E7%94%B2%E5%9F%BA%E9%85%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%EF%BC%8C%E5%85%B6%E5%9C%A8%E5%8C%96%E5%AD%A6%E9%9D%A2%E4%B8%8A%E5%A4%9A%E5%85%B7%E6%9C%89%E5%A6%82%E4%B8%8B%E7%89%B9%E6%80%A7%EF%BC%9A
This compound has a certain chemical activity because it contains specific atomic groups. Among them, 2,6-dioxybenzyl and acetamide groups interact to affect its overall chemical properties. In common organic solvents, it has a certain solubility and can be dissolved in some polar organic solvents such as ethanol and acetone, which is due to the interaction force between polar groups and solvent molecules in its molecular structure.
From the perspective of reactivity, some groups in this compound can participate in a variety of chemical reactions. Such as acetamide moiety, under appropriate conditions, hydrolysis can occur to break amide bonds and generate corresponding amine and carboxylic acid derivatives. At the same time, the oxygen atom in 2,6-dioxobenzyl has a certain nucleophilicity, which can react with electrophilic reagents in a specific reaction system, so as to realize the modification and transformation of molecular structure.
Furthermore, due to the presence of benzene ring structure in the molecule, it is endowed with certain stability and aromatic related properties. The conjugate system of benzene ring makes the molecule have a unique electron cloud distribution, which is also reflected in physical properties such as light and electricity. For example, under the irradiation of light of a specific wavelength, optical phenomena such as electron transition may occur, which provides the basis for its potential applications in optical materials and other fields. Its chemical properties are influenced by the synergy effect of each group, and it can exhibit a variety of chemical behaviors under different reaction conditions and environments, providing rich possibilities for the study of organic synthesis and related fields.
This compound has a certain chemical activity because it contains specific atomic groups. Among them, 2,6-dioxybenzyl and acetamide groups interact to affect its overall chemical properties. In common organic solvents, it has a certain solubility and can be dissolved in some polar organic solvents such as ethanol and acetone, which is due to the interaction force between polar groups and solvent molecules in its molecular structure.
From the perspective of reactivity, some groups in this compound can participate in a variety of chemical reactions. Such as acetamide moiety, under appropriate conditions, hydrolysis can occur to break amide bonds and generate corresponding amine and carboxylic acid derivatives. At the same time, the oxygen atom in 2,6-dioxobenzyl has a certain nucleophilicity, which can react with electrophilic reagents in a specific reaction system, so as to realize the modification and transformation of molecular structure.
Furthermore, due to the presence of benzene ring structure in the molecule, it is endowed with certain stability and aromatic related properties. The conjugate system of benzene ring makes the molecule have a unique electron cloud distribution, which is also reflected in physical properties such as light and electricity. For example, under the irradiation of light of a specific wavelength, optical phenomena such as electron transition may occur, which provides the basis for its potential applications in optical materials and other fields. Its chemical properties are influenced by the synergy effect of each group, and it can exhibit a variety of chemical behaviors under different reaction conditions and environments, providing rich possibilities for the study of organic synthesis and related fields.
What are the uses of 2- ((2,6-dichlorophenyl) amino) -phenylacetate carboxymethyl ester
2 - ((2,6 -dioxybenzyl) amino) -benzyl benzoate, this compound has its uses in many fields.
In the field of medicinal chemistry, it may be used as an important pharmaceutical intermediate. With its unique chemical structure, it can combine with other active groups through specific chemical reactions to synthesize drug molecules with specific pharmacological activities. For example, through the modification and modification of its structure, new therapeutic drugs for specific disease targets can be developed, such as anti-cancer drugs, antiviral drugs, etc. With the help of its structure and activity relationship, it provides a key basic raw material for the development of new drugs.
In the field of organic synthesis, it is an extremely important building block. Due to its multiple reactive check points, it can participate in many complex organic synthesis reactions, such as nucleophilic substitution reactions, electrophilic substitution reactions, etc. Through these reactions, chemists can ingeniously construct more complex and diverse organic molecular structures, laying the foundation for the synthesis of organic materials with special functions and structures.
In the field of materials science, it also has potential applications. Through appropriate polymerization reactions or modifications, it may be introduced into the structure of polymer materials, giving the material special properties, such as improving the optical properties and thermal stability of the material. It may be possible to prepare functional materials with unique application value in optoelectronic devices, sensors, etc.
In conclusion, 2 - ((2,6 -dioxybenzyl) amino) -benzyl benzoate has shown important application potential in many important fields such as medicine, organic synthesis and materials science. With the continuous deepening of research, it is expected to explore more innovative uses.
In the field of medicinal chemistry, it may be used as an important pharmaceutical intermediate. With its unique chemical structure, it can combine with other active groups through specific chemical reactions to synthesize drug molecules with specific pharmacological activities. For example, through the modification and modification of its structure, new therapeutic drugs for specific disease targets can be developed, such as anti-cancer drugs, antiviral drugs, etc. With the help of its structure and activity relationship, it provides a key basic raw material for the development of new drugs.
In the field of organic synthesis, it is an extremely important building block. Due to its multiple reactive check points, it can participate in many complex organic synthesis reactions, such as nucleophilic substitution reactions, electrophilic substitution reactions, etc. Through these reactions, chemists can ingeniously construct more complex and diverse organic molecular structures, laying the foundation for the synthesis of organic materials with special functions and structures.
In the field of materials science, it also has potential applications. Through appropriate polymerization reactions or modifications, it may be introduced into the structure of polymer materials, giving the material special properties, such as improving the optical properties and thermal stability of the material. It may be possible to prepare functional materials with unique application value in optoelectronic devices, sensors, etc.
In conclusion, 2 - ((2,6 -dioxybenzyl) amino) -benzyl benzoate has shown important application potential in many important fields such as medicine, organic synthesis and materials science. With the continuous deepening of research, it is expected to explore more innovative uses.
What is the synthesis method of 2- ((2,6-dichlorophenyl) amino) -phenylacetate carboxymethyl ester
To prepare 2 - ((2,6 - difluorobenzyl) amino) -benzyl benzoate, the method is as follows:
First take an appropriate amount of 2,6 - difluorobenzyl amine and place it in a clean reactor. Take another appropriate amount of 2 - benzyl halobenzoate, slowly add it to the kettle, and add an appropriate amount of alkali, such as potassium carbonate or sodium carbonate, as an acid binding agent. Select a suitable organic solvent, such as N, N - dimethylformamide (DMF) or acetonitrile, so that the reactants are fully dissolved and evenly dispersed.
Warm up to a suitable reaction temperature, about 60 - 80 ° C, maintain this temperature and continue to stir to make the reaction proceed smoothly. During the reaction, the reaction progress was regularly monitored by thin-layer chromatography (TLC) to observe the ratio of raw materials to products. When the raw materials are almost completely reacted, the heating is stopped and the reaction system is allowed to cool naturally.
Then, pour the reaction solution into an appropriate amount of water and extract it with ethyl acetate for multiple times. The organic phases were combined, washed with water and saturated salt water in turn, and dried with anhydrous sodium sulfate to remove the moisture.
Then, the organic solvent was evaporated under reduced pressure with a rotary evaporator to obtain a crude product. The crude product was purified by column chromatography, and a suitable eluent was selected, such as a mixture of petroleum ether and ethyl acetate, and eluted in a proportional layer. The eluent containing the target product is collected, and the solvent is evaporated under reduced pressure again to obtain pure 2 - ((2,6 -difluorobenzyl) amino) -benzyl benzoate.
This synthesis method is simple to operate, relatively mild conditions, and the yield is considerable. It can be applied to small-scale preparation in the laboratory or appropriately amplified for industrial production.
First take an appropriate amount of 2,6 - difluorobenzyl amine and place it in a clean reactor. Take another appropriate amount of 2 - benzyl halobenzoate, slowly add it to the kettle, and add an appropriate amount of alkali, such as potassium carbonate or sodium carbonate, as an acid binding agent. Select a suitable organic solvent, such as N, N - dimethylformamide (DMF) or acetonitrile, so that the reactants are fully dissolved and evenly dispersed.
Warm up to a suitable reaction temperature, about 60 - 80 ° C, maintain this temperature and continue to stir to make the reaction proceed smoothly. During the reaction, the reaction progress was regularly monitored by thin-layer chromatography (TLC) to observe the ratio of raw materials to products. When the raw materials are almost completely reacted, the heating is stopped and the reaction system is allowed to cool naturally.
Then, pour the reaction solution into an appropriate amount of water and extract it with ethyl acetate for multiple times. The organic phases were combined, washed with water and saturated salt water in turn, and dried with anhydrous sodium sulfate to remove the moisture.
Then, the organic solvent was evaporated under reduced pressure with a rotary evaporator to obtain a crude product. The crude product was purified by column chromatography, and a suitable eluent was selected, such as a mixture of petroleum ether and ethyl acetate, and eluted in a proportional layer. The eluent containing the target product is collected, and the solvent is evaporated under reduced pressure again to obtain pure 2 - ((2,6 -difluorobenzyl) amino) -benzyl benzoate.
This synthesis method is simple to operate, relatively mild conditions, and the yield is considerable. It can be applied to small-scale preparation in the laboratory or appropriately amplified for industrial production.
What are the market prospects for 2- ((2,6-dichlorophenyl) amino) -phenylacetate carboxymethyl esters?
2-%28%282%2C6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29-%E8%8B%AF%E4%B9%99%E9%85%B8%E7%BE%A7%E7%94%B2%E5%9F%BA%E9%85%AF%E7%9A%84%E5%B8%82%E5%9C%BA%E5%89%8D%E6%99%AF%E5%A6%82%E4%BD%95%3F%2C this is a chemically related substance, in order to know its market prospect, it is necessary to look at many factors.
In the field of medicine, 2 - ((2,6 -dioxybenzyl) amino) -benzoic acid methyl benzyl esters may have unique pharmacological activities. Nowadays, the pharmaceutical market is increasingly in demand for innovative drugs. If this substance has significant efficacy after research and can pass rigorous clinical trials, it may emerge in the development of new drugs, and the market prospect is broad.
In the field of materials science, such compounds may be used as raw materials for new materials. With the advancement of science and technology, the demand for high-performance and special functional materials is increasing. If it can give materials unique properties, such as excellent stability, conductivity or optical properties, it will gain a place in the electronic and optical materials market.
However, its marketing activities also face challenges. R & D costs are high, and a lot of capital is required from laboratory research to industrial production. And the market competition is fierce, with many similar or alternative products. To open up the market, it is necessary to have significant advantages, such as higher cost performance and better performance.
In summary, 2 - ((2,6 - dioxybenzyl) amino) - benzoic acid methyl benzyl ester if it can overcome the research and development and marketing activities of the problem, give full play to their own characteristics, the market prospects are considerable; On the contrary, if unable to meet the challenge, the market expansion road or full of difficulties.
In the field of medicine, 2 - ((2,6 -dioxybenzyl) amino) -benzoic acid methyl benzyl esters may have unique pharmacological activities. Nowadays, the pharmaceutical market is increasingly in demand for innovative drugs. If this substance has significant efficacy after research and can pass rigorous clinical trials, it may emerge in the development of new drugs, and the market prospect is broad.
In the field of materials science, such compounds may be used as raw materials for new materials. With the advancement of science and technology, the demand for high-performance and special functional materials is increasing. If it can give materials unique properties, such as excellent stability, conductivity or optical properties, it will gain a place in the electronic and optical materials market.
However, its marketing activities also face challenges. R & D costs are high, and a lot of capital is required from laboratory research to industrial production. And the market competition is fierce, with many similar or alternative products. To open up the market, it is necessary to have significant advantages, such as higher cost performance and better performance.
In summary, 2 - ((2,6 - dioxybenzyl) amino) - benzoic acid methyl benzyl ester if it can overcome the research and development and marketing activities of the problem, give full play to their own characteristics, the market prospects are considerable; On the contrary, if unable to meet the challenge, the market expansion road or full of difficulties.
What are the relevant safety considerations for 2- ((2,6-dichlorophenyl) amino) -phenylacetate carboxymethyl esters?
2-%28%282%2C6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29-%E8%8B%AF%E4%B9%99%E9%85%B8%E7%BE%A7%E7%94%B2%E5%9F%BA%E9%85%AF%E6%9C%89%E5%85%B3%E5%AE%89%E5%85%A8%E4%B9%8B%E4%BA%8B, you need to be cautious. This is a class of chemical substances, which is related to life and health and environmental safety, so the following things cannot be ignored.
The first to bear the brunt, such substances have certain toxicity. It may invade the human body through breathing, skin contact, ingestion, etc., damaging the nervous system, liver, kidneys and many other organs, causing headaches, dizziness, nausea, vomiting, fatigue and other diseases, even life-threatening. Therefore, when exposed, protective equipment, such as protective clothing, gloves, masks, goggles, etc. must be worn to prevent contact with the human body.
Furthermore, such substances are not stable and are affected by heat, light, vibration, etc., or cause decomposition and explosion. When storing, store in a cool, dry and ventilated place, away from fire, heat and oxidants, and store properly according to regulations to prevent accidents.
Repeat, such substances are also harmful to the environment. They may pollute soil, water sources and air, endangering ecological balance. After use, the residue cannot be discarded at will, and must be properly disposed of in accordance with relevant regulations to reduce the impact on the environment.
In addition, the user must have professional training, familiar with its nature, use, safety precautions, etc. When operating, strictly follow the regulations and do not make any claims. And the workplace must be prepared with emergency rescue equipment and medicines for emergencies.
In short, when it comes to 2-%28%282%6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29-%E8%8B%AF%E4%B9%99%E9%85%B8%E7%BE%A7%E7%94%B2%E5%9F%BA%E9%85%AF, from use to storage, to processing, all need to be cautious, and must not be negligent, so that the security is safe.
The first to bear the brunt, such substances have certain toxicity. It may invade the human body through breathing, skin contact, ingestion, etc., damaging the nervous system, liver, kidneys and many other organs, causing headaches, dizziness, nausea, vomiting, fatigue and other diseases, even life-threatening. Therefore, when exposed, protective equipment, such as protective clothing, gloves, masks, goggles, etc. must be worn to prevent contact with the human body.
Furthermore, such substances are not stable and are affected by heat, light, vibration, etc., or cause decomposition and explosion. When storing, store in a cool, dry and ventilated place, away from fire, heat and oxidants, and store properly according to regulations to prevent accidents.
Repeat, such substances are also harmful to the environment. They may pollute soil, water sources and air, endangering ecological balance. After use, the residue cannot be discarded at will, and must be properly disposed of in accordance with relevant regulations to reduce the impact on the environment.
In addition, the user must have professional training, familiar with its nature, use, safety precautions, etc. When operating, strictly follow the regulations and do not make any claims. And the workplace must be prepared with emergency rescue equipment and medicines for emergencies.
In short, when it comes to 2-%28%282%6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29-%E8%8B%AF%E4%B9%99%E9%85%B8%E7%BE%A7%E7%94%B2%E5%9F%BA%E9%85%AF, from use to storage, to processing, all need to be cautious, and must not be negligent, so that the security is safe.
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