Linshang Chemical
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2-Chloro-4-Methoxybenzene-1,3-Diol
Linshang Chemical
|
HS Code |
148551 |
| Chemical Formula | C7H7ClO3 |
| Molecular Weight | 174.58 |
| Appearance | Solid (predicted) |
| Boiling Point | 346.1°C at 760 mmHg (predicted) |
| Melting Point | 162 - 164°C |
| Flash Point | 163.1°C (predicted) |
| Density | 1.459 g/cm³ (predicted) |
| Solubility In Water | Slightly soluble (predicted) |
| Logp | 1.13 (predicted) |
| Pka | 7.79 (predicted) |
As an accredited 2-Chloro-4-Methoxybenzene-1,3-Diol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2 - chloro - 4 - methoxybenzene - 1,3 - diol packaged in a sealed plastic bottle. |
| Storage | 2 - Chloro - 4 - methoxybenzene - 1,3 - diol should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and exposure to air, which could lead to degradation. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions. |
| Shipping | 2 - chloro - 4 - methoxybenzene - 1,3 - diol should be shipped in sealed, corrosion - resistant containers. Ensure compliance with chemical transportation regulations, with proper labeling indicating its nature to guarantee safe transit. |
Competitive 2-Chloro-4-Methoxybenzene-1,3-Diol prices that fit your budget—flexible terms and customized quotes for every order.
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2-chloro-4-methoxybenzene-1, what are the chemical properties of 3-diol?
2-Chloro-4-methoxybenzene-1,3-diol, this is an organic compound with interesting chemical properties.
Looking at its structure, the chlorine atom, methoxy group and two hydroxyl groups coexist on the benzene ring. The hydroxyl group is active and can participate in many chemical reactions. First, esterification can occur, just like meeting an acid, the hydrogen atom in the hydroxyl group dehydrates from the carboxyl group of the acid to form esters. Second, due to the conjugate system of the benzene ring, the hydroxyl group is easily oxidized, just like when encountering strong oxidants, or transformed into oxidation products such as quinones.
Chlorine atoms also have characteristics. It can undergo nucleophilic substitution reaction under appropriate conditions. If nucleophilic reagents are attacked, chlorine atoms may be replaced. This reaction is often an important step in organic synthesis.
Methoxy groups have an effect on the electron cloud density of the benzene ring. It has the electron supply effect, which increases the density of the adjacent and para-electron clouds of the benzene ring, so that the electrophilic substitution reaction is more likely to occur at these locations.
This compound may have potential uses in pharmaceutical chemistry, materials science and other fields due to its multiple active groups. Its unique chemical properties provide scientists with opportunities to explore new reactions and develop new substances.
Looking at its structure, the chlorine atom, methoxy group and two hydroxyl groups coexist on the benzene ring. The hydroxyl group is active and can participate in many chemical reactions. First, esterification can occur, just like meeting an acid, the hydrogen atom in the hydroxyl group dehydrates from the carboxyl group of the acid to form esters. Second, due to the conjugate system of the benzene ring, the hydroxyl group is easily oxidized, just like when encountering strong oxidants, or transformed into oxidation products such as quinones.
Chlorine atoms also have characteristics. It can undergo nucleophilic substitution reaction under appropriate conditions. If nucleophilic reagents are attacked, chlorine atoms may be replaced. This reaction is often an important step in organic synthesis.
Methoxy groups have an effect on the electron cloud density of the benzene ring. It has the electron supply effect, which increases the density of the adjacent and para-electron clouds of the benzene ring, so that the electrophilic substitution reaction is more likely to occur at these locations.
This compound may have potential uses in pharmaceutical chemistry, materials science and other fields due to its multiple active groups. Its unique chemical properties provide scientists with opportunities to explore new reactions and develop new substances.
2-chloro-4-methoxybenzene-1, what are the physical properties of 3-diol
2-Chloro-4-methoxybenzene-1,3-diol is one of the organic compounds. Its physical properties are quite important and are listed as follows:
First words appearance, this compound is often white to light yellow solid, and the texture is fine, like a fine powder or crystalline aggregate, which is the appearance that can be seen by the human eye.
When it comes to melting point, it is usually in a specific temperature range. The exact value of its melting point depends on the purity of the compound and the conditions for determination. Generally speaking, its melting point is mostly in the category of melting points of common organic compounds, which can provide an important basis for the identification and purity determination of the substance.
As for the boiling point, it is also one of the key physical properties. However, its boiling point is also affected by factors such as pressure. Under standard pressure conditions, the boiling point presents a certain value, which plays a crucial role in the separation and purification of compounds, and is related to the setting of conditions for distillation and other operations.
In terms of solubility, 2-chloro-4-methoxybenzene-1,3-diol behaves differently in organic solvents. It exhibits good solubility in some common organic solvents, such as ethanol and acetone, and can be uniformly dispersed to form a uniform solution. However, in water, its solubility is relatively limited. This property is closely related to the groups contained in its molecular structure. The interaction of chlorine atoms, methoxy groups, and diol groups together determines its dissolution behavior in different solvents.
In addition, the density of the compound is also one of its physical properties. Although its exact density value needs to be accurately determined experimentally, its density characteristics are of great significance in the calculation of the relationship between mass and volume of the substance, as well as in the study of the distribution of the mixed system.
In summary, the physical properties of 2-chloro-4-methoxybenzene-1,3-diol, such as appearance, melting point, boiling point, solubility, and density, are interrelated and have various uses. They are all indispensable factors to consider in the research of organic chemistry, the process of chemical production, and the practical application in related fields.
First words appearance, this compound is often white to light yellow solid, and the texture is fine, like a fine powder or crystalline aggregate, which is the appearance that can be seen by the human eye.
When it comes to melting point, it is usually in a specific temperature range. The exact value of its melting point depends on the purity of the compound and the conditions for determination. Generally speaking, its melting point is mostly in the category of melting points of common organic compounds, which can provide an important basis for the identification and purity determination of the substance.
As for the boiling point, it is also one of the key physical properties. However, its boiling point is also affected by factors such as pressure. Under standard pressure conditions, the boiling point presents a certain value, which plays a crucial role in the separation and purification of compounds, and is related to the setting of conditions for distillation and other operations.
In terms of solubility, 2-chloro-4-methoxybenzene-1,3-diol behaves differently in organic solvents. It exhibits good solubility in some common organic solvents, such as ethanol and acetone, and can be uniformly dispersed to form a uniform solution. However, in water, its solubility is relatively limited. This property is closely related to the groups contained in its molecular structure. The interaction of chlorine atoms, methoxy groups, and diol groups together determines its dissolution behavior in different solvents.
In addition, the density of the compound is also one of its physical properties. Although its exact density value needs to be accurately determined experimentally, its density characteristics are of great significance in the calculation of the relationship between mass and volume of the substance, as well as in the study of the distribution of the mixed system.
In summary, the physical properties of 2-chloro-4-methoxybenzene-1,3-diol, such as appearance, melting point, boiling point, solubility, and density, are interrelated and have various uses. They are all indispensable factors to consider in the research of organic chemistry, the process of chemical production, and the practical application in related fields.
2-chloro-4-methoxybenzene-1, what is the common synthesis method of 3-diol?
To prepare 2-chloro-4-methoxybenzene-1,3-diol, there are several common methods as follows.
First, use an appropriate phenolic compound as the starting material. First, the hydroxyl group of the phenol is properly protected to prevent it from being affected in the subsequent reaction. Then, using a halogenation reaction, chlorine atoms are introduced. A suitable halogenation reagent can be selected, and under suitable reaction conditions, the chlorine atom can accurately replace the hydrogen atom at a specific position on the benzene ring. Then, through a methoxylation reaction, a methoxy group is introduced. This step requires the selection of a suitable methoxylation reagent and reaction conditions to ensure the smooth progress of the reaction and good selectivity. Finally, the group that previously protected the hydroxyl group is removed, and after appropriate post-treatment, the target product 2-chloro-4-methoxybenzene-1,3-diol can be obtained.
Second, it can also start from the derivative of benzene. First construct the benzene ring structure containing methoxy group, which can be achieved by the corresponding nucleophilic substitution reaction. Subsequently, chlorine atoms are introduced at specific positions. This step requires precise control of the reaction conditions to ensure the accuracy of the chlorine atom substitution position. Then through appropriate oxidation or other conversion reactions, hydroxyl groups are introduced at specific positions in the benzene ring to generate the desired diol structure. During this period, the intermediates in each step of the reaction need to be carefully separated and purified to ensure the purity of the final product.
Or, take some natural products or existing benzene-containing compounds as the starting materials, and gradually introduce chlorine atoms, methoxy groups and diol structures through clever chemical transformation according to their existing structural characteristics. This approach requires in-depth knowledge of the reactivity and selectivity of the starting materials in order to effectively achieve the synthesis of the target product. In short, the synthesis of 2-chloro-4-methoxybenzene-1,3-diol requires careful design of the reaction route according to the actual situation, and strict control of the reaction conditions at each step.
First, use an appropriate phenolic compound as the starting material. First, the hydroxyl group of the phenol is properly protected to prevent it from being affected in the subsequent reaction. Then, using a halogenation reaction, chlorine atoms are introduced. A suitable halogenation reagent can be selected, and under suitable reaction conditions, the chlorine atom can accurately replace the hydrogen atom at a specific position on the benzene ring. Then, through a methoxylation reaction, a methoxy group is introduced. This step requires the selection of a suitable methoxylation reagent and reaction conditions to ensure the smooth progress of the reaction and good selectivity. Finally, the group that previously protected the hydroxyl group is removed, and after appropriate post-treatment, the target product 2-chloro-4-methoxybenzene-1,3-diol can be obtained.
Second, it can also start from the derivative of benzene. First construct the benzene ring structure containing methoxy group, which can be achieved by the corresponding nucleophilic substitution reaction. Subsequently, chlorine atoms are introduced at specific positions. This step requires precise control of the reaction conditions to ensure the accuracy of the chlorine atom substitution position. Then through appropriate oxidation or other conversion reactions, hydroxyl groups are introduced at specific positions in the benzene ring to generate the desired diol structure. During this period, the intermediates in each step of the reaction need to be carefully separated and purified to ensure the purity of the final product.
Or, take some natural products or existing benzene-containing compounds as the starting materials, and gradually introduce chlorine atoms, methoxy groups and diol structures through clever chemical transformation according to their existing structural characteristics. This approach requires in-depth knowledge of the reactivity and selectivity of the starting materials in order to effectively achieve the synthesis of the target product. In short, the synthesis of 2-chloro-4-methoxybenzene-1,3-diol requires careful design of the reaction route according to the actual situation, and strict control of the reaction conditions at each step.
2-chloro-4-methoxybenzene-1, 3-diol is used in which areas
2-Chloro-4-methoxybenzene-1,3-diol, this compound is useful in medicine, chemical synthesis and other fields.
In the field of medicine, it can be a key raw material for the creation of new antibacterial drugs. Due to its unique structure, the compound exhibits inhibitory activity against some bacteria and fungi. By further exploring its mechanism of interaction with microorganisms, it may be possible to develop antibacterial agents with good efficacy and small side effects for the treatment of various infectious diseases.
In the field of chemical synthesis, it is also an important intermediate. It can be converted into compounds with more complex structures through a series of chemical reactions. If it reacts with specific reagents to construct materials with special optical and electrical properties, it may be useful in the field of optoelectronics to produce organic Light Emitting Diode materials with excellent performance and improve the image quality and efficiency of display devices.
In addition, in the research and development of agricultural chemicals, 2-chloro-4-methoxybenzene-1,3-diol also has potential. It may be developed into a new type of pesticide. With its biological activity against certain pests, it can achieve effective prevention and control of crop diseases and pests, and ensure crop yield and quality. In short, this compound has potential application value in many fields. With the deepening of research, its application prospect may be broader.
In the field of medicine, it can be a key raw material for the creation of new antibacterial drugs. Due to its unique structure, the compound exhibits inhibitory activity against some bacteria and fungi. By further exploring its mechanism of interaction with microorganisms, it may be possible to develop antibacterial agents with good efficacy and small side effects for the treatment of various infectious diseases.
In the field of chemical synthesis, it is also an important intermediate. It can be converted into compounds with more complex structures through a series of chemical reactions. If it reacts with specific reagents to construct materials with special optical and electrical properties, it may be useful in the field of optoelectronics to produce organic Light Emitting Diode materials with excellent performance and improve the image quality and efficiency of display devices.
In addition, in the research and development of agricultural chemicals, 2-chloro-4-methoxybenzene-1,3-diol also has potential. It may be developed into a new type of pesticide. With its biological activity against certain pests, it can achieve effective prevention and control of crop diseases and pests, and ensure crop yield and quality. In short, this compound has potential application value in many fields. With the deepening of research, its application prospect may be broader.
2-chloro-4-methoxybenzene-1, what is the market outlook for 3-diol?
2-Chloro-4-methoxybenzene-1,3-diol, this is an organic compound. Looking at its market prospects, it needs to be studied more carefully.
From the pharmaceutical field, organic compounds are often key intermediates in drug synthesis. The specific chemical structure of 2-chloro-4-methoxybenzene-1,3-diol may play a role in the creation of some drugs. There is a strong demand for characteristic structural intermediates in pharmaceutical research and development. If they can fit the design of specific drug targets, they may have a place in the process of new drug development, and the market prospect is also promising.
In the field of materials science, many organic compounds can be specially treated and modified to become materials with excellent performance. 2-Chloro-4-methoxybenzene-1,3-diol may have the potential to participate in the synthesis of special functional materials, such as optoelectronic materials. With the rapid development of science and technology, the demand for new functional materials is increasing. If it can emerge in this field, the market demand may increase significantly.
However, its market prospect also faces challenges. The synthesis process of organic compounds is always complex, and cost control is a major problem. If the synthesis process cannot be optimized and the production cost is reduced, it may be difficult to gain an advantage in the market competition. Furthermore, the market is increasingly demanding the safety and environmental friendliness of compounds. 2-chloro-4-methoxybenzene-1,3-diol needs to meet relevant regulations and standards, otherwise it may be rejected by the market.
In summary, although 2-chloro-4-methoxybenzene-1,3-diol has potential application value in the fields of medicine and materials, in order to open up a good market prospect, it is still necessary to overcome many difficulties such as synthesis cost, safety and environmental protection.
From the pharmaceutical field, organic compounds are often key intermediates in drug synthesis. The specific chemical structure of 2-chloro-4-methoxybenzene-1,3-diol may play a role in the creation of some drugs. There is a strong demand for characteristic structural intermediates in pharmaceutical research and development. If they can fit the design of specific drug targets, they may have a place in the process of new drug development, and the market prospect is also promising.
In the field of materials science, many organic compounds can be specially treated and modified to become materials with excellent performance. 2-Chloro-4-methoxybenzene-1,3-diol may have the potential to participate in the synthesis of special functional materials, such as optoelectronic materials. With the rapid development of science and technology, the demand for new functional materials is increasing. If it can emerge in this field, the market demand may increase significantly.
However, its market prospect also faces challenges. The synthesis process of organic compounds is always complex, and cost control is a major problem. If the synthesis process cannot be optimized and the production cost is reduced, it may be difficult to gain an advantage in the market competition. Furthermore, the market is increasingly demanding the safety and environmental friendliness of compounds. 2-chloro-4-methoxybenzene-1,3-diol needs to meet relevant regulations and standards, otherwise it may be rejected by the market.
In summary, although 2-chloro-4-methoxybenzene-1,3-diol has potential application value in the fields of medicine and materials, in order to open up a good market prospect, it is still necessary to overcome many difficulties such as synthesis cost, safety and environmental protection.
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