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N-(Aminoiminomethyl)-2,6-Dichlorobenzeneacetamide Hydrochloride
Linshang Chemical
|
HS Code |
299029 |
| Chemical Name | N-(Aminoiminomethyl)-2,6-Dichlorobenzeneacetamide Hydrochloride |
As an accredited N-(Aminoiminomethyl)-2,6-Dichlorobenzeneacetamide Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram pack of N-(aminoiminomethyl)-2,6 - dichlorobenzeneacetamide Hydrochloride in sealed container. |
| Storage | Store N-(aminoiminomethyl)-2,6 - dichlorobenzeneacetamide Hydrochloride in a cool, dry place, away from direct sunlight and heat sources. Keep it in a tightly - sealed container to prevent moisture absorption and contact with air, which could potentially cause degradation. Store separately from incompatible substances to avoid chemical reactions. |
| Shipping | N-(aminoiminomethyl)-2,6 - dichlorobenzeneacetamide Hydrochloride is shipped in well - sealed, corrosion - resistant containers. Special care is taken to comply with chemical transport regulations to ensure safe transit. |
Competitive N-(Aminoiminomethyl)-2,6-Dichlorobenzeneacetamide Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.
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What is the chemical structure of N- (aminoiminomethyl) -2, 6-dichlorobenzeneacetamide Hydrochloride?
The chemical structure of "N- (aminomethyl) -2,6-dichlorophenylacetamide hydrochloride" is an important topic in the field of organic chemistry. Its structure is composed of several parts.
Looking at its main body, it is based on the benzene ring, and at the 2nd and 6th positions of the benzene ring, each connected to a chlorine atom. The substitution of this chlorine atom gives the compound specific physical and chemical properties. On one side of the benzene ring, the acetamide structure is connected. This acetamide part contains a carbonyl group and an amino group. The conjugation effect of the two affects the stability and reactivity of the molecule.
The key point is that the N atom is connected to the "aminomethyl". In this part, the amino group is connected to the iminomethyl group, and the iminomethyl group is connected to the N atom. The existence of carbon and nitrogen double bonds in the iminomethyl group and the active hydrogen of the amino group make this structure unique in chemical reactions. The form of
hydrochloride forms a corresponding salt due to the interaction of the compound with hydrochloric acid. The formation of this salt greatly changes the solubility and stability of the compound. In the field of pharmaceutical chemistry and other fields, it is often used to optimize the properties of drugs. The various parts of the overall structure interact and cooperate to shape the unique chemical behavior and properties of the compound.
Looking at its main body, it is based on the benzene ring, and at the 2nd and 6th positions of the benzene ring, each connected to a chlorine atom. The substitution of this chlorine atom gives the compound specific physical and chemical properties. On one side of the benzene ring, the acetamide structure is connected. This acetamide part contains a carbonyl group and an amino group. The conjugation effect of the two affects the stability and reactivity of the molecule.
The key point is that the N atom is connected to the "aminomethyl". In this part, the amino group is connected to the iminomethyl group, and the iminomethyl group is connected to the N atom. The existence of carbon and nitrogen double bonds in the iminomethyl group and the active hydrogen of the amino group make this structure unique in chemical reactions. The form of
hydrochloride forms a corresponding salt due to the interaction of the compound with hydrochloric acid. The formation of this salt greatly changes the solubility and stability of the compound. In the field of pharmaceutical chemistry and other fields, it is often used to optimize the properties of drugs. The various parts of the overall structure interact and cooperate to shape the unique chemical behavior and properties of the compound.
What are the main uses of N- (aminoiminomethyl) -2, 6-dichlorobenzeneacetamide Hydrochloride?
N- (Aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride has a wide range of uses. In the field of medicine, it is often used as an important intermediate to assist in the synthesis of a variety of drugs. For example, when developing drugs for specific inflammation or infection, the compound can participate in key reaction steps with its unique chemical structure, laying the foundation for the creation of new drugs with excellent efficacy.
In the chemical industry, it also plays a key role in the organic synthesis process. It can be used as a starting material or reaction aid to participate in the construction of complex organic molecules. Due to its special functional groups, it can guide the reaction in a specific direction and assist in the synthesis of materials with specific properties, such as special polymers, which contribute significantly to material modification and optimization.
Furthermore, at the level of scientific research and exploration, N- (Aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride provides an effective tool for scientists to study new chemical reaction mechanisms and explore new synthesis paths. With in-depth exploration of its chemical properties, researchers can expand the boundaries of chemical knowledge and promote the development and progress of organic chemistry and other disciplines.
In the chemical industry, it also plays a key role in the organic synthesis process. It can be used as a starting material or reaction aid to participate in the construction of complex organic molecules. Due to its special functional groups, it can guide the reaction in a specific direction and assist in the synthesis of materials with specific properties, such as special polymers, which contribute significantly to material modification and optimization.
Furthermore, at the level of scientific research and exploration, N- (Aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride provides an effective tool for scientists to study new chemical reaction mechanisms and explore new synthesis paths. With in-depth exploration of its chemical properties, researchers can expand the boundaries of chemical knowledge and promote the development and progress of organic chemistry and other disciplines.
What are the physical properties of N- (aminoiminomethyl) -2, 6-dichlorobenzeneacetamide Hydrochloride?
N- (Amino-iminomethyl) -2,6-dichlorophenylacetamide hydrochloride, this is an organic compound. Its physical properties are quite critical and are of great significance in both chemical research and practical applications.
Looking at its appearance, under normal temperature and pressure, it is mostly white to white crystalline powder. This form is conducive to storage and use, and the powder state increases the surface area of the substance. In chemical reactions, the reaction can be more sufficient and efficient.
Solubility is also an important physical property. This substance exhibits a certain solubility in water, but the specific solubility is affected by many factors such as temperature and pH of the solution. Generally speaking, when the temperature increases, its solubility in water may increase. In organic solvents, such as ethanol and acetone, it also has certain solubility properties, but the degree of solubility varies depending on the properties of the solvent. This solubility property is extremely important for its separation, purification and reaction medium selection in various chemical processes.
In terms of melting point, the compound has a specific melting point value. Melting point is a key indicator for identification and purity determination. Pure N- (aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride has a relatively fixed melting point. If it contains impurities, the melting point may decrease and the melting range will also become wider. Therefore, by accurately measuring the melting point, its purity status can be preliminarily inferred.
In addition, its density is also a physical parameter. Although the specific density value varies according to the measurement conditions, its relative density can reflect the density of the substance, which has a certain impact on the packaging, transportation, and distribution of the substance in a specific system.
The physical properties of this compound are interrelated and affect, and in many fields such as chemical synthesis, drug development, and material preparation, these properties need to be fully considered in order to achieve the best application effect.
Looking at its appearance, under normal temperature and pressure, it is mostly white to white crystalline powder. This form is conducive to storage and use, and the powder state increases the surface area of the substance. In chemical reactions, the reaction can be more sufficient and efficient.
Solubility is also an important physical property. This substance exhibits a certain solubility in water, but the specific solubility is affected by many factors such as temperature and pH of the solution. Generally speaking, when the temperature increases, its solubility in water may increase. In organic solvents, such as ethanol and acetone, it also has certain solubility properties, but the degree of solubility varies depending on the properties of the solvent. This solubility property is extremely important for its separation, purification and reaction medium selection in various chemical processes.
In terms of melting point, the compound has a specific melting point value. Melting point is a key indicator for identification and purity determination. Pure N- (aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride has a relatively fixed melting point. If it contains impurities, the melting point may decrease and the melting range will also become wider. Therefore, by accurately measuring the melting point, its purity status can be preliminarily inferred.
In addition, its density is also a physical parameter. Although the specific density value varies according to the measurement conditions, its relative density can reflect the density of the substance, which has a certain impact on the packaging, transportation, and distribution of the substance in a specific system.
The physical properties of this compound are interrelated and affect, and in many fields such as chemical synthesis, drug development, and material preparation, these properties need to be fully considered in order to achieve the best application effect.
What is the preparation method of N- (aminoiminomethyl) -2, 6-dichlorobenzeneacetamide Hydrochloride?
To prepare N- (aminoiminomethyl) -2,6-dichlorophenylacetamide hydrochloride, the ancient method may have the following numbers.
First take 2,6-dichlorophenylacetonitrile, this is the base material. In a suitable container, an alcohol solvent such as ethanol is preferred. Acid is used as a catalyst, hydrochloric acid is commonly used, and an appropriate amount is added. Heat to make the temperature, control it at a moderate degree, about 50 to 70 degrees Celsius, and let it hydrolyze. During hydrolysis, the nitrile group gradually converts into an amide group to give 2,6-dichlorophenylacetamide. This step takes a long time, often several hours, and requires time to add stirring to ensure a uniform reaction.
Take the prepared 2,6-dichlorophenylacetamide and put it into another container. Adjust its pH with an appropriate base, such as sodium carbonate, etc. Then add cyanamide, which is the key to introducing aminoiminomethyl. In a water-soluble system, heat it to 60 to 80 degrees Celsius, and react for several hours. Cyanamide reacts with the carbonyl group of 2,6-dichlorophenylacetamide in a series of nucleophilic additions, resulting in N- (aminoiminomethyl) -2,6-dichlorophenylacetamide.
At the end, prepare its hydrochloride. Dissolve N- (aminoiminomethyl) -2,6-dichlorophenylacetamide into an alcohol solvent and slowly pass into hydrogen chloride gas. Hydrogen chloride and amino groups combine to form a salt and precipitate in the solution. After the reaction is completed, filter, wash, and dry to obtain pure N- (aminoiminomethyl) -2,6 -dichlorophenylacetamide hydrochloride. Each step of the reaction should pay attention to temperature, pH, and the proportion of materials. A slight difference may affect the yield and purity.
First take 2,6-dichlorophenylacetonitrile, this is the base material. In a suitable container, an alcohol solvent such as ethanol is preferred. Acid is used as a catalyst, hydrochloric acid is commonly used, and an appropriate amount is added. Heat to make the temperature, control it at a moderate degree, about 50 to 70 degrees Celsius, and let it hydrolyze. During hydrolysis, the nitrile group gradually converts into an amide group to give 2,6-dichlorophenylacetamide. This step takes a long time, often several hours, and requires time to add stirring to ensure a uniform reaction.
Take the prepared 2,6-dichlorophenylacetamide and put it into another container. Adjust its pH with an appropriate base, such as sodium carbonate, etc. Then add cyanamide, which is the key to introducing aminoiminomethyl. In a water-soluble system, heat it to 60 to 80 degrees Celsius, and react for several hours. Cyanamide reacts with the carbonyl group of 2,6-dichlorophenylacetamide in a series of nucleophilic additions, resulting in N- (aminoiminomethyl) -2,6-dichlorophenylacetamide.
At the end, prepare its hydrochloride. Dissolve N- (aminoiminomethyl) -2,6-dichlorophenylacetamide into an alcohol solvent and slowly pass into hydrogen chloride gas. Hydrogen chloride and amino groups combine to form a salt and precipitate in the solution. After the reaction is completed, filter, wash, and dry to obtain pure N- (aminoiminomethyl) -2,6 -dichlorophenylacetamide hydrochloride. Each step of the reaction should pay attention to temperature, pH, and the proportion of materials. A slight difference may affect the yield and purity.
N- (aminoiminomethyl) -2, 6-dichlorobenzeneacetamide Hydrochloride What are the precautions during use?
N- (Aminoiminomethyl) - 2,6-dichlorophenylacetamide hydrochloride, this is a chemical substance. During use, there are several important items to pay attention to.
First safety protection. Because it is a chemical, it may be toxic and corrosive to a certain extent. Be sure to wear appropriate protective equipment, such as laboratory clothes, gloves, goggles, etc., to prevent it from coming into contact with the skin and eyes. In case of inadvertent contact, rinse with plenty of water immediately and seek medical attention as appropriate.
Times and operating environment. It needs to be operated in a well-ventilated place to prevent its volatile gases from accumulating in a limited space and causing hazards such as poisoning. The operating table should also be kept clean to avoid impurities from mixing in, affecting its chemical properties or causing unexpected reactions.
The other is the storage condition. It should be stored in a dry, cool and ventilated place, away from fire sources and oxidants. Due to its chemical nature or activity, improper storage or deterioration will affect the use effect and even cause danger.
The weighing and dosage should also be accurate. According to the needs of the experiment or production, weigh accurately to avoid excess or insufficient. Excessive or waste, pollution, or insufficient or insufficient reaction, unable to achieve the intended purpose.
Proper disposal of residues and waste after use. Do not dump at will, and need to be disposed of in accordance with chemical waste treatment specifications to prevent environmental pollution.
In addition, it is necessary to be familiar with its chemical properties, reaction characteristics and emergency treatment methods before use, so as to effectively use this chemical substance under the premise of ensuring safety.
First safety protection. Because it is a chemical, it may be toxic and corrosive to a certain extent. Be sure to wear appropriate protective equipment, such as laboratory clothes, gloves, goggles, etc., to prevent it from coming into contact with the skin and eyes. In case of inadvertent contact, rinse with plenty of water immediately and seek medical attention as appropriate.
Times and operating environment. It needs to be operated in a well-ventilated place to prevent its volatile gases from accumulating in a limited space and causing hazards such as poisoning. The operating table should also be kept clean to avoid impurities from mixing in, affecting its chemical properties or causing unexpected reactions.
The other is the storage condition. It should be stored in a dry, cool and ventilated place, away from fire sources and oxidants. Due to its chemical nature or activity, improper storage or deterioration will affect the use effect and even cause danger.
The weighing and dosage should also be accurate. According to the needs of the experiment or production, weigh accurately to avoid excess or insufficient. Excessive or waste, pollution, or insufficient or insufficient reaction, unable to achieve the intended purpose.
Proper disposal of residues and waste after use. Do not dump at will, and need to be disposed of in accordance with chemical waste treatment specifications to prevent environmental pollution.
In addition, it is necessary to be familiar with its chemical properties, reaction characteristics and emergency treatment methods before use, so as to effectively use this chemical substance under the premise of ensuring safety.
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