Linshang Chemical
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3-Chloro-N'-Hydroxybenzenecarboximidamide
Linshang Chemical
|
HS Code |
824167 |
| Chemical Formula | C7H7ClN2O |
| Molecular Weight | 170.596 g/mol |
| Appearance | Solid (predicted) |
As an accredited 3-Chloro-N'-Hydroxybenzenecarboximidamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 3 - chloro - N’ - hydroxybenzenecarboximidamide in a sealed chemical - grade bag. |
| Storage | 3 - Chloro - N’ - hydroxybenzenecarboximidamide should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and direct sunlight to prevent decomposition. Store in a tightly - sealed container to avoid contact with moisture and air, which could potentially react with the chemical and affect its quality. |
| Shipping | 3 - chloro - N’ - hydroxybenzenecarboximidamide should be shipped in well - sealed containers, following hazardous chemical regulations. Ensure proper labeling and handling to prevent spills, with transportation in vehicles equipped for chemical transport. |
Competitive 3-Chloro-N'-Hydroxybenzenecarboximidamide prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 3-Chloro-N'-Hydroxybenzenecarboximidamide 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 3-chloro-n hydroxybenzenecarboximidamide?
3 - chloro - N '- hydroxybenzenecarboximidamide is one of the organic compounds. Its molecular structure can be analyzed as follows:
This compound is based on the benzene ring, and above the benzene ring, it is connected to a chlorine atom (-Cl) at the third position. This chlorine atom has the properties of halogenated hydrocarbons and can participate in various reactions such as nucleophilic substitution.
There is also a carboxyamidine group (-C (= NH) NH -2) connected to the benzene ring, and then at the nitrogen atom (N') of the carboxyamidine group, it is connected to a hydroxy group (-OH). The combination of this carboxyamidine group and hydroxyl group gives the compound unique chemical properties.
Carboxyamidine is basically basic and can form salts with acids; while hydroxyl groups not only have a certain nucleophilicity, but also participate in the formation of hydrogen bonds, which has a great impact on molecular interactions.
The structure of this compound makes it possible to have potential applications in organic synthesis, pharmaceutical chemistry and other fields. For example, in drug development, this unique structure may provide the possibility of specific binding to biological targets, and then exhibit specific physiological activities.
In summary, the chemical structure of 3-chloro-N '-hydroxybenzenecarboximidamide is composed of phenyl ring, chlorine atom, carboxyamidine group and hydroxyl group attached to nitrogen atom. Each part interacts to determine its chemical properties and potential uses.
This compound is based on the benzene ring, and above the benzene ring, it is connected to a chlorine atom (-Cl) at the third position. This chlorine atom has the properties of halogenated hydrocarbons and can participate in various reactions such as nucleophilic substitution.
There is also a carboxyamidine group (-C (= NH) NH -2) connected to the benzene ring, and then at the nitrogen atom (N') of the carboxyamidine group, it is connected to a hydroxy group (-OH). The combination of this carboxyamidine group and hydroxyl group gives the compound unique chemical properties.
Carboxyamidine is basically basic and can form salts with acids; while hydroxyl groups not only have a certain nucleophilicity, but also participate in the formation of hydrogen bonds, which has a great impact on molecular interactions.
The structure of this compound makes it possible to have potential applications in organic synthesis, pharmaceutical chemistry and other fields. For example, in drug development, this unique structure may provide the possibility of specific binding to biological targets, and then exhibit specific physiological activities.
In summary, the chemical structure of 3-chloro-N '-hydroxybenzenecarboximidamide is composed of phenyl ring, chlorine atom, carboxyamidine group and hydroxyl group attached to nitrogen atom. Each part interacts to determine its chemical properties and potential uses.
What are the physical properties of 3-chloro-n hydroxybenzenecarboximidamide?
3 - chloro - N '- hydroxybenzenecarboximidamide is one of the organic compounds. Looking at its physical properties, under normal conditions, it is mostly white to white solid. The value of its melting point often varies slightly depending on the purity of the sample, probably within a certain range. This property can be used for identification and purity determination.
When it comes to solubility, this compound exhibits a specific solubility behavior in common organic solvents. In polar organic solvents, such as methanol and ethanol, it has a certain solubility and can form a uniform solution. Due to the interaction force between molecules, the solute and solvent molecules interact to dissolve. However, in non-polar organic solvents, such as n-hexane and benzene, their solubility is poor, due to the difference in molecular polarity, making it difficult for the two to miscible with each other.
Its density is also one of the important physical properties. Although the exact value or the measurement conditions vary slightly, it is roughly in a specific range. This property is related to its distribution and behavior in different media.
In addition, the appearance properties of the compound are stable. Under general environmental conditions, without special chemical reaction conditions, it is not easy to undergo significant physical changes. The comprehensive performance of its physical properties not only lays the foundation for its application in organic synthesis, drug research and development, but also provides an important basis for relevant researchers to deeply understand its chemical behavior and potential uses. Studying its physical properties can provide indispensable information for subsequent chemical operations, separation and purification, and product quality control.
When it comes to solubility, this compound exhibits a specific solubility behavior in common organic solvents. In polar organic solvents, such as methanol and ethanol, it has a certain solubility and can form a uniform solution. Due to the interaction force between molecules, the solute and solvent molecules interact to dissolve. However, in non-polar organic solvents, such as n-hexane and benzene, their solubility is poor, due to the difference in molecular polarity, making it difficult for the two to miscible with each other.
Its density is also one of the important physical properties. Although the exact value or the measurement conditions vary slightly, it is roughly in a specific range. This property is related to its distribution and behavior in different media.
In addition, the appearance properties of the compound are stable. Under general environmental conditions, without special chemical reaction conditions, it is not easy to undergo significant physical changes. The comprehensive performance of its physical properties not only lays the foundation for its application in organic synthesis, drug research and development, but also provides an important basis for relevant researchers to deeply understand its chemical behavior and potential uses. Studying its physical properties can provide indispensable information for subsequent chemical operations, separation and purification, and product quality control.
What are the common uses of 3-chloro-n hydroxybenzenecarboximidamide?
3-chloro-N '-hydroxybenzenecarboximidamide, Chinese name 3-chloro-N' -hydroxybenzamidine, this is an organic compound. Its common uses are as follows:
** Pharmaceutical synthesis field **:
The construction of many drug molecules is often used as a key intermediate. Due to the functional groups contained in the molecule, it can participate in various chemical reactions, such as amidation reaction, nucleophilic substitution reaction, etc., to construct complex drug structures. For example, when developing specific antibacterial drugs, 3-chloro-N '-hydroxybenzamidine can react with other compounds containing active groups to synthesize new substances with antibacterial activity. This new substance may inhibit bacterial cell wall synthesis or interfere with bacterial protein metabolism, thus achieving antibacterial effect.
** Field of Organic Synthetic Chemistry **:
1. As an important synthetic building block, it is used to build various organic compounds with special structures and properties. Because of its unique chemical structure and reactivity, it can participate in the construction of aromatic rings, heterocyclic synthesis and other reactions. For example, by reacting with suitable reagents, nitrogen-containing heterocyclic structures can be formed, which are widely found in many natural products and functional materials.
2. For the design and synthesis of new organic ligands. After organic ligands are complexed with metal ions, they are widely used in catalytic reactions, materials science and other fields. 3-Chloro-N '-hydroxybenzamidine derived ligands, or due to the presence of chlorine atoms and hydroxyl groups, exhibit unique coordination ability and spatial structure, which in turn affect the catalytic properties and material properties of metal complexes.
** Materials Science Field **:
1. In the preparation of functional polymer materials, 3-chloro-N' -hydroxybenzamidine can be introduced into the polymer chain as a monomer or modifier. For example, copolymerization with ethylene monomers to prepare polymers with special functions. Its introduction may endow polymers with antibacterial, chelating metal ions and other properties, thereby broadening the application of polymers in food packaging, water treatment and other fields.
2. In the preparation of metal-organic framework (MOF) materials, it can be used as an organic linker. With its ability to coordinate with metal ions, MOF materials with specific pore structures and functions are constructed. Such materials have broad prospects in gas adsorption and separation, catalysis, etc., such as high selective adsorption ability for specific gases, or as high-efficiency catalyst carriers.
** Pharmaceutical synthesis field **:
The construction of many drug molecules is often used as a key intermediate. Due to the functional groups contained in the molecule, it can participate in various chemical reactions, such as amidation reaction, nucleophilic substitution reaction, etc., to construct complex drug structures. For example, when developing specific antibacterial drugs, 3-chloro-N '-hydroxybenzamidine can react with other compounds containing active groups to synthesize new substances with antibacterial activity. This new substance may inhibit bacterial cell wall synthesis or interfere with bacterial protein metabolism, thus achieving antibacterial effect.
** Field of Organic Synthetic Chemistry **:
1. As an important synthetic building block, it is used to build various organic compounds with special structures and properties. Because of its unique chemical structure and reactivity, it can participate in the construction of aromatic rings, heterocyclic synthesis and other reactions. For example, by reacting with suitable reagents, nitrogen-containing heterocyclic structures can be formed, which are widely found in many natural products and functional materials.
2. For the design and synthesis of new organic ligands. After organic ligands are complexed with metal ions, they are widely used in catalytic reactions, materials science and other fields. 3-Chloro-N '-hydroxybenzamidine derived ligands, or due to the presence of chlorine atoms and hydroxyl groups, exhibit unique coordination ability and spatial structure, which in turn affect the catalytic properties and material properties of metal complexes.
** Materials Science Field **:
1. In the preparation of functional polymer materials, 3-chloro-N' -hydroxybenzamidine can be introduced into the polymer chain as a monomer or modifier. For example, copolymerization with ethylene monomers to prepare polymers with special functions. Its introduction may endow polymers with antibacterial, chelating metal ions and other properties, thereby broadening the application of polymers in food packaging, water treatment and other fields.
2. In the preparation of metal-organic framework (MOF) materials, it can be used as an organic linker. With its ability to coordinate with metal ions, MOF materials with specific pore structures and functions are constructed. Such materials have broad prospects in gas adsorption and separation, catalysis, etc., such as high selective adsorption ability for specific gases, or as high-efficiency catalyst carriers.
What are the synthesis methods of 3-chloro-n hydroxybenzenecarboximidamide?
To prepare 3 - chloro - N '- hydroxybenzenecarboximidamide, we can think of it from the common organic synthesis path.
First, 3 - chlorobenzoic acid can be started. First, 3 - chlorobenzoic acid is converted into 3 - chlorobenzoyl chloride, which can be reacted with sulfuryl chloride ($SOCl_2 $). Under heating conditions, the carboxyl group is converted into an acyl chloride group. The chemical equation is: 3 dollars - chlorobenzoic acid + SOCl_2\ stackrel {\ Delta} {\ longrightarrow} 3 - chlorobenzoyl chloride + SO_2\ uparrow + HCl\ uparrow $.
Then, 3-chlorobenzoyl chloride reacts with hydroxylamine ($NH_2OH $) to obtain the target product 3-chloro-N '- hydroxybenzenecarboximidamide, and the reaction formula is: 3 dollars-chlorobenzoyl chloride + NH_2OH\ longrightarrow 3-chloro-N' - hydroxybenzenecarboximidamide + HCl $.
Second, 3-chlorobenzonitrile can also be used as the starting material. 3-chlorobenzonitrile is first reacted with hydroxylamine under alkaline conditions to form an intermediate, and then acidified to obtain the target product. The reaction under alkaline conditions is roughly: 3 dollars - chlorobenzonitrile + NH_2OH + OH ^ -\ longrightarrow intermediate $, and the intermediate is acidified to obtain 3 - chloro - N '- hydroxybenzenecarboximidamide.
These two paths are feasible methods for synthesizing 3 - chloro - N' - hydroxybenzenecarboximidamide. In actual operation, it needs to be selected according to factors such as the availability of raw materials and the difficulty of controlling the reaction conditions.
First, 3 - chlorobenzoic acid can be started. First, 3 - chlorobenzoic acid is converted into 3 - chlorobenzoyl chloride, which can be reacted with sulfuryl chloride ($SOCl_2 $). Under heating conditions, the carboxyl group is converted into an acyl chloride group. The chemical equation is: 3 dollars - chlorobenzoic acid + SOCl_2\ stackrel {\ Delta} {\ longrightarrow} 3 - chlorobenzoyl chloride + SO_2\ uparrow + HCl\ uparrow $.
Then, 3-chlorobenzoyl chloride reacts with hydroxylamine ($NH_2OH $) to obtain the target product 3-chloro-N '- hydroxybenzenecarboximidamide, and the reaction formula is: 3 dollars-chlorobenzoyl chloride + NH_2OH\ longrightarrow 3-chloro-N' - hydroxybenzenecarboximidamide + HCl $.
Second, 3-chlorobenzonitrile can also be used as the starting material. 3-chlorobenzonitrile is first reacted with hydroxylamine under alkaline conditions to form an intermediate, and then acidified to obtain the target product. The reaction under alkaline conditions is roughly: 3 dollars - chlorobenzonitrile + NH_2OH + OH ^ -\ longrightarrow intermediate $, and the intermediate is acidified to obtain 3 - chloro - N '- hydroxybenzenecarboximidamide.
These two paths are feasible methods for synthesizing 3 - chloro - N' - hydroxybenzenecarboximidamide. In actual operation, it needs to be selected according to factors such as the availability of raw materials and the difficulty of controlling the reaction conditions.
What are the precautions for using 3-chloro-n hydroxybenzenecarboximidamide?
3 - chloro - N '- hydroxybenzenecarboximidamide, this is an organic compound, there are several points to be paid attention to during use.
First safety protection. This compound may be toxic and irritating, and be sure to wear appropriate protective equipment when operating. Such as wearing protective gloves to prevent it from contacting the skin, causing adverse consequences such as skin allergies and burns; wearing protective glasses to protect the eyes from its splash damage; also wearing a mask to avoid inhaling its dust or volatile gases to prevent respiratory damage, causing cough, asthma and other symptoms.
Furthermore, pay attention to the operating environment. It should be operated in a well-ventilated place. If conditions permit, it is best to operate in a fume hood, which can disperse the volatile gas in time, reduce the concentration of the compound in the air, and reduce the harm to the human body. At the same time, the operating table must be kept clean and tidy to avoid other sundries and the compound from contaminating each other, affecting its properties or causing unexpected reactions.
Third, accurately control the dosage. According to experimental or production needs, accurately measure the compound to avoid too much or too little dosage. Excessive dosage, or excessive reaction, generating unnecessary by-products, may also cause waste of resources; if the dosage is too small, the reaction may not achieve the desired effect. When measuring, choose appropriate measuring tools and follow correct operating specifications to ensure accurate measurement.
Fourth, properly store. The compound should be stored in a dry and cool place, away from fire sources and oxidants. Due to its active chemical properties, it may be exposed to heat, open flames or oxidants, or there is a danger of combustion or explosion. At the same time, it is necessary to make a good mark, indicating the name, specification, date and other information of the compound, so that it can be used and managed in the future.
In addition, after use, the remaining compounds and related waste should be properly disposed of according to regulations. It must not be discarded at will to prevent environmental pollution. Generally speaking, appropriate treatment methods should be selected according to their chemical properties, such as neutralization, dilution, recycling, etc., to ensure that they meet environmental protection requirements.
First safety protection. This compound may be toxic and irritating, and be sure to wear appropriate protective equipment when operating. Such as wearing protective gloves to prevent it from contacting the skin, causing adverse consequences such as skin allergies and burns; wearing protective glasses to protect the eyes from its splash damage; also wearing a mask to avoid inhaling its dust or volatile gases to prevent respiratory damage, causing cough, asthma and other symptoms.
Furthermore, pay attention to the operating environment. It should be operated in a well-ventilated place. If conditions permit, it is best to operate in a fume hood, which can disperse the volatile gas in time, reduce the concentration of the compound in the air, and reduce the harm to the human body. At the same time, the operating table must be kept clean and tidy to avoid other sundries and the compound from contaminating each other, affecting its properties or causing unexpected reactions.
Third, accurately control the dosage. According to experimental or production needs, accurately measure the compound to avoid too much or too little dosage. Excessive dosage, or excessive reaction, generating unnecessary by-products, may also cause waste of resources; if the dosage is too small, the reaction may not achieve the desired effect. When measuring, choose appropriate measuring tools and follow correct operating specifications to ensure accurate measurement.
Fourth, properly store. The compound should be stored in a dry and cool place, away from fire sources and oxidants. Due to its active chemical properties, it may be exposed to heat, open flames or oxidants, or there is a danger of combustion or explosion. At the same time, it is necessary to make a good mark, indicating the name, specification, date and other information of the compound, so that it can be used and managed in the future.
In addition, after use, the remaining compounds and related waste should be properly disposed of according to regulations. It must not be discarded at will to prevent environmental pollution. Generally speaking, appropriate treatment methods should be selected according to their chemical properties, such as neutralization, dilution, recycling, etc., to ensure that they meet environmental protection requirements.
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