Linshang Chemical
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2-Chloro-1,3-Dihydroxybenzene
Linshang Chemical
|
HS Code |
812859 |
| Chemical Formula | C6H5ClO2 |
| Molar Mass | 144.555 g/mol |
| Appearance | Solid |
As an accredited 2-Chloro-1,3-Dihydroxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2 - chloro - 1,3 - dihydroxybenzene packaged in a sealed, air - tight bottle. |
| Storage | 2 - chloro - 1,3 - dihydroxybenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and evaporation. It's best stored in a dedicated chemical storage cabinet, separated from incompatible substances to avoid potential reactions. |
| Shipping | 2 - chloro - 1,3 - dihydroxybenzene should be shipped in well - sealed, corrosion - resistant containers. Ensure compliance with hazardous chemical shipping regulations, with proper labeling indicating its nature to prevent any risks during transit. |
Competitive 2-Chloro-1,3-Dihydroxybenzene prices that fit your budget—flexible terms and customized quotes for every order.
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What is the Chinese name of 2-chloro-1,3-dihydroxybenzene?
2-Chloro-1,3-dihydroxybenzene, its Chinese name is 2-chloro-resorcinol.
The name of this organic compound, "2-chloro", is due to the presence of a chlorine atom at position 2 of the benzene ring. Chlorine atoms, a genus of halogen elements, are active and often play an important role in organic reactions. And "1,3-dihydroxy", it is indicated that there is a hydroxyl group connected to position 1 and position 3 of the benzene ring. Hydroxyl groups, which are hydrophilic, can make the compound have different solubility properties in some media, and can participate in many chemical reactions, such as esterification and substitution. The
resorcinol is an isomer of resorcinol. Catechol has three isomers, o, m, and p, which are mesomorphic states. resorcinol has applications in industry, medicine, dyes and other fields. And 2-chloro-resorcinol, due to the introduction of chlorine atoms, has different properties than resorcinol, or has unique efficacy in specific reactions and applications. It may be used as an intermediate in organic synthesis and converted into more complex organic compounds with specific functions through a series of reactions. In the field of medicine, or due to structural characteristics, it has potential biological activity; in the dye industry, it may be able to assist in the color and stability of dyes with its structure.
The name of this organic compound, "2-chloro", is due to the presence of a chlorine atom at position 2 of the benzene ring. Chlorine atoms, a genus of halogen elements, are active and often play an important role in organic reactions. And "1,3-dihydroxy", it is indicated that there is a hydroxyl group connected to position 1 and position 3 of the benzene ring. Hydroxyl groups, which are hydrophilic, can make the compound have different solubility properties in some media, and can participate in many chemical reactions, such as esterification and substitution. The
resorcinol is an isomer of resorcinol. Catechol has three isomers, o, m, and p, which are mesomorphic states. resorcinol has applications in industry, medicine, dyes and other fields. And 2-chloro-resorcinol, due to the introduction of chlorine atoms, has different properties than resorcinol, or has unique efficacy in specific reactions and applications. It may be used as an intermediate in organic synthesis and converted into more complex organic compounds with specific functions through a series of reactions. In the field of medicine, or due to structural characteristics, it has potential biological activity; in the dye industry, it may be able to assist in the color and stability of dyes with its structure.
What are the main uses of 2-chloro-1,3-dihydroxybenzene?
2-Chloro-1,3-dihydroxybenzene, this substance has a wide range of uses. In the field of medicine, it is often used as a raw material for creating antibacterial and anti-inflammatory medicines. Because of its special chemical structure, it can be combined with other substances by chemical methods to create drugs with unique curative effects, making great contributions to treating diseases and diseases.
In the field of materials, it is also used for extraordinary purposes. It can be used as a key ingredient in the synthesis of special functional materials. For example, the preparation of polymer materials with good antioxidant properties, which are skillfully reacted and integrated into the molecular structure to greatly increase the stability of the material, and are used in many high-end products, such as protective materials for aerospace equipment parts, to ensure long-term durability of the equipment in complex environments.
In chemical production, it is an important intermediate. With its structural activity, it is converted into a variety of high value-added chemical products through various reaction paths. Or through substitution, addition and other reactions, a series of fine chemicals are derived, which contribute to the expansion and enrichment of the chemical industry chain. It has far-reaching significance in industrial production and is related to the output and quality improvement of many chemical products.
In the field of materials, it is also used for extraordinary purposes. It can be used as a key ingredient in the synthesis of special functional materials. For example, the preparation of polymer materials with good antioxidant properties, which are skillfully reacted and integrated into the molecular structure to greatly increase the stability of the material, and are used in many high-end products, such as protective materials for aerospace equipment parts, to ensure long-term durability of the equipment in complex environments.
In chemical production, it is an important intermediate. With its structural activity, it is converted into a variety of high value-added chemical products through various reaction paths. Or through substitution, addition and other reactions, a series of fine chemicals are derived, which contribute to the expansion and enrichment of the chemical industry chain. It has far-reaching significance in industrial production and is related to the output and quality improvement of many chemical products.
What are the physical properties of 2-chloro-1,3-dihydroxybenzene?
2-Chloro-1,3-dihydroxybenzene, this is an organic compound. Its physical properties are quite important, and it is related to many chemical uses and characteristics.
First of all, the appearance is often white to light yellow crystalline powder, delicate and pure, and its pure texture can be seen from the perspective, like a natural micro-treasure. Its melting point is in a specific range, about 100-105 ° C. At this temperature limit, the solid phase will quietly transform into the liquid phase. This is the key node of the change of material state, just like a temperature code given by nature.
In terms of solubility, in water, its solubility is limited, just like a fish that is difficult to fully integrate into the vast ocean, and only part of its body is compatible with water; however, in organic solvents, such as ethanol, acetone, etc., it can show good solubility, as if the wanderers return to a suitable hometown and disperse freely and harmoniously.
Volatility, because of its stable structure, volatility is weak, just like a calm person, does not easily show an impulsive state, can maintain a relatively stable form of existence under normal conditions, and is not easy to escape with air.
As for the density, it is about 1.4 - 1.5 g/cm ³, which makes it have a unique weight texture among similar compounds, as if it occupies a specific weight position on the balance of matter.
2-chloro-1,3-dihydroxybenzene These physical properties play an indispensable role in organic synthesis, drug research and development, and are like the cornerstone of building a magnificent chemical building, supporting many important chemical processes and applications.
First of all, the appearance is often white to light yellow crystalline powder, delicate and pure, and its pure texture can be seen from the perspective, like a natural micro-treasure. Its melting point is in a specific range, about 100-105 ° C. At this temperature limit, the solid phase will quietly transform into the liquid phase. This is the key node of the change of material state, just like a temperature code given by nature.
In terms of solubility, in water, its solubility is limited, just like a fish that is difficult to fully integrate into the vast ocean, and only part of its body is compatible with water; however, in organic solvents, such as ethanol, acetone, etc., it can show good solubility, as if the wanderers return to a suitable hometown and disperse freely and harmoniously.
Volatility, because of its stable structure, volatility is weak, just like a calm person, does not easily show an impulsive state, can maintain a relatively stable form of existence under normal conditions, and is not easy to escape with air.
As for the density, it is about 1.4 - 1.5 g/cm ³, which makes it have a unique weight texture among similar compounds, as if it occupies a specific weight position on the balance of matter.
2-chloro-1,3-dihydroxybenzene These physical properties play an indispensable role in organic synthesis, drug research and development, and are like the cornerstone of building a magnificent chemical building, supporting many important chemical processes and applications.
What are the chemical properties of 2-chloro-1,3-dihydroxybenzene?
2-Chloro-1,3-dihydroxybenzene is one of the organic compounds. It has unique chemical properties, so let me tell you one by one.
The first to bear the brunt is the property of its phenolic hydroxyl group. The compound contains dihydroxyl groups, which are highly active and acidic. It can react with bases, such as with sodium hydroxide, and the hydrogen of the phenolic hydroxyl group can be replaced by sodium ions to form the corresponding sodium phenol salt, which is a typical reaction of phenolic compounds. Phenolic hydroxyl groups are also easily oxidized, and in the air, they can be gradually oxidized, causing the color to change from colorless or light to dark.
Furthermore, its chlorine atoms are also reactive. Chlorine atoms can undergo substitution reactions. If nucleophiles come in, chlorine atoms can be replaced by nucleophiles. For example, when reacted with sodium alcohol, chlorine atoms can be replaced by alkoxy groups to form corresponding ether compounds; when reacted with ammonia or amines, nitrogen-containing derivatives can be formed.
In addition, the compound has aromatic properties due to its benzene ring structure. Aromatic electrophilic substitution reactions can occur, such as halogenation, nitrification, sulfonation, etc. Under appropriate conditions, other groups can be introduced into the benzene ring, resulting in more abundant compound structures and properties.
In the field of organic synthesis, 2-chloro-1,3-dihydroxybenzene is often used as an important intermediate. With the reactivity of phenolic hydroxyl groups and chlorine atoms, complex organic molecular structures can be constructed through various chemical reactions, providing key starting materials for drug synthesis, materials science and other fields. It is an indispensable substance in organic chemistry research and application.
The first to bear the brunt is the property of its phenolic hydroxyl group. The compound contains dihydroxyl groups, which are highly active and acidic. It can react with bases, such as with sodium hydroxide, and the hydrogen of the phenolic hydroxyl group can be replaced by sodium ions to form the corresponding sodium phenol salt, which is a typical reaction of phenolic compounds. Phenolic hydroxyl groups are also easily oxidized, and in the air, they can be gradually oxidized, causing the color to change from colorless or light to dark.
Furthermore, its chlorine atoms are also reactive. Chlorine atoms can undergo substitution reactions. If nucleophiles come in, chlorine atoms can be replaced by nucleophiles. For example, when reacted with sodium alcohol, chlorine atoms can be replaced by alkoxy groups to form corresponding ether compounds; when reacted with ammonia or amines, nitrogen-containing derivatives can be formed.
In addition, the compound has aromatic properties due to its benzene ring structure. Aromatic electrophilic substitution reactions can occur, such as halogenation, nitrification, sulfonation, etc. Under appropriate conditions, other groups can be introduced into the benzene ring, resulting in more abundant compound structures and properties.
In the field of organic synthesis, 2-chloro-1,3-dihydroxybenzene is often used as an important intermediate. With the reactivity of phenolic hydroxyl groups and chlorine atoms, complex organic molecular structures can be constructed through various chemical reactions, providing key starting materials for drug synthesis, materials science and other fields. It is an indispensable substance in organic chemistry research and application.
What are the preparation methods of 2-chloro-1,3-dihydroxybenzene?
2-Chloro-1,3-dihydroxybenzene is one of the most important in the field of organic compounds. Its preparation methods are diverse, and I will describe them in detail.
First, it can be obtained from the halogenation reaction of specific phenolic compounds. First take the appropriate phenolic substances, place them in the reaction vessel, and add an appropriate amount of halogenating reagents, such as chlorine-containing halogenating agents. Control the reaction conditions, such as temperature, reaction time, and the proportion of reactants. If the temperature is too high, it may cause side reactions and lead to impure products; if the temperature is too low, the reaction will be slow and the efficiency will be poor. After this halogenation reaction, chlorine atoms are introduced into the specific positions of phenolic compounds, resulting in 2-chloro-1,3-dihydroxybenzene.
Second, the derivative of benzene is used as the starting material and prepared by multi-step reaction. First, the benzene derivative is introduced and modified with specific groups to make it have a suitable reaction check point. Subsequently, through hydroxylation reaction, the hydroxyl group is introduced at a specific position in the benzene ring. Then the halogenation step is performed to precisely introduce chlorine atoms. Although this method is complicated, the structure of the product can be finely adjusted to obtain high-purity 2-chloro-1,3-dihydroxybenzene.
Third, it is prepared by catalytic reaction. Selecting a suitable catalyst can significantly improve the reaction rate and selectivity. In a specific reaction system, the reactants react according to a predetermined path under the action of the catalyst to generate the target product. The choice of catalyst is crucial, and its activity, selectivity and stability all have a profound impact on the effectiveness of the reaction.
When preparing 2-chloro-1,3-dihydroxybenzene, it is necessary to carefully control the reaction conditions and select appropriate raw materials and methods. In this way, the ideal product can be obtained to meet the application needs of different fields.
First, it can be obtained from the halogenation reaction of specific phenolic compounds. First take the appropriate phenolic substances, place them in the reaction vessel, and add an appropriate amount of halogenating reagents, such as chlorine-containing halogenating agents. Control the reaction conditions, such as temperature, reaction time, and the proportion of reactants. If the temperature is too high, it may cause side reactions and lead to impure products; if the temperature is too low, the reaction will be slow and the efficiency will be poor. After this halogenation reaction, chlorine atoms are introduced into the specific positions of phenolic compounds, resulting in 2-chloro-1,3-dihydroxybenzene.
Second, the derivative of benzene is used as the starting material and prepared by multi-step reaction. First, the benzene derivative is introduced and modified with specific groups to make it have a suitable reaction check point. Subsequently, through hydroxylation reaction, the hydroxyl group is introduced at a specific position in the benzene ring. Then the halogenation step is performed to precisely introduce chlorine atoms. Although this method is complicated, the structure of the product can be finely adjusted to obtain high-purity 2-chloro-1,3-dihydroxybenzene.
Third, it is prepared by catalytic reaction. Selecting a suitable catalyst can significantly improve the reaction rate and selectivity. In a specific reaction system, the reactants react according to a predetermined path under the action of the catalyst to generate the target product. The choice of catalyst is crucial, and its activity, selectivity and stability all have a profound impact on the effectiveness of the reaction.
When preparing 2-chloro-1,3-dihydroxybenzene, it is necessary to carefully control the reaction conditions and select appropriate raw materials and methods. In this way, the ideal product can be obtained to meet the application needs of different fields.
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