Linshang Chemical
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1,2-Dichloro-5-Methoxy-3-Methylbenzene
Linshang Chemical
|
HS Code |
837084 |
| Chemical Formula | C8H8Cl2O |
| Molar Mass | 191.054 g/mol |
| Solubility In Water | Low, as it is an organic compound with non - polar groups |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone, benzene |
| Vapor Pressure | Low, due to its relatively high molar mass and lack of highly volatile functional groups |
| Stability | Stable under normal conditions, but can react with strong oxidizing agents |
As an accredited 1,2-Dichloro-5-Methoxy-3-Methylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1,2 - dichloro - 5 - methoxy - 3 - methylbenzene packaged in a sealed plastic bottle. |
| Storage | 1,2 - Dichloro - 5 - methoxy - 3 - methylbenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent leakage and vapor release. Store it separately from oxidizing agents, strong acids, and bases to avoid potential chemical reactions. |
| Shipping | 1,2 - Dichloro - 5 - methoxy - 3 - methylbenzene is shipped in sealed, corrosion - resistant containers. It adheres to strict chemical transportation regulations, ensuring secure transit to prevent spills and environmental/health risks. |
Competitive 1,2-Dichloro-5-Methoxy-3-Methylbenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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What are the physical properties of 1,2-dichloro-5-methoxy-3-methylbenzene?
1%2C2+-+%E4%BA%8C%E6%B0%AF+-+5+-+%E7%94%B2%E6%B0%A7%E5%9F%BA+-+3+-+%E7%94%B2%E5%9F%BA%E8%8B%AF%E7%9A%84%E5%85%B7%E4%BD%93%E5%88%86%E5%AD%90%E5%BC%8F%E4%B8%BAC
HO, this is an organic compound. Its physical properties are as follows:
Looking at its properties, it is mostly a colorless to light yellow oily liquid under normal conditions. After light or long-term storage, or due to oxidation, the color becomes slightly darker.
Smell its smell and have a unique aromatic smell. It is often used in the field of fragrances as a fragrance enhancer, which can give the product a unique and charming fragrance.
Its boiling point is about a specific temperature range. Due to the intermolecular force of the compound, a specific heat is required to transform it from liquid to gaseous. This boiling point characteristic is of great significance in separation, purification and related process operations.
Measuring its density, it is slightly lighter than water. If mixed with water, it can be observed to float on the water surface. This property requires much attention when it comes to the treatment of the mixed system of the substance and water.
Exploring its solubility, it is slightly soluble in water, which is caused by the difference between the polarity of water molecules and the polarity of the organic molecule; however, it can be soluble in many organic solvents, such as ethanol, ether, etc. According to the principle of similarity compatibility, molecules with similar polarities are easy to dissolve each other. This solubility characteristic is crucial in its extraction, separation and reaction solvent selection.
From the perspective of its volatility, it is volatile to a certain extent. In an open environment, it will gradually evaporate from liquid to gaseous. This characteristic should be properly considered during storage and use to prevent losses due to volatilization or safety issues.
HO, this is an organic compound. Its physical properties are as follows:
Looking at its properties, it is mostly a colorless to light yellow oily liquid under normal conditions. After light or long-term storage, or due to oxidation, the color becomes slightly darker.
Smell its smell and have a unique aromatic smell. It is often used in the field of fragrances as a fragrance enhancer, which can give the product a unique and charming fragrance.
Its boiling point is about a specific temperature range. Due to the intermolecular force of the compound, a specific heat is required to transform it from liquid to gaseous. This boiling point characteristic is of great significance in separation, purification and related process operations.
Measuring its density, it is slightly lighter than water. If mixed with water, it can be observed to float on the water surface. This property requires much attention when it comes to the treatment of the mixed system of the substance and water.
Exploring its solubility, it is slightly soluble in water, which is caused by the difference between the polarity of water molecules and the polarity of the organic molecule; however, it can be soluble in many organic solvents, such as ethanol, ether, etc. According to the principle of similarity compatibility, molecules with similar polarities are easy to dissolve each other. This solubility characteristic is crucial in its extraction, separation and reaction solvent selection.
From the perspective of its volatility, it is volatile to a certain extent. In an open environment, it will gradually evaporate from liquid to gaseous. This characteristic should be properly considered during storage and use to prevent losses due to volatilization or safety issues.
What are the chemical properties of 1,2-dichloro-5-methoxy-3-methylbenzene?
1% 2C2 + - + dioxy + - + 5 + - + methoxy + - + 3 + - + methylbenzene has a wide range of chemical properties. This substance has the commonality of aromatic hydrocarbons, the benzene ring is stable, and electrophilic substitution reactions can occur, such as halogenation, nitration, sulfonation, etc. Taking halogenation as an example, under the action of catalysts such as iron halide, halogens such as chlorine and bromine can replace hydrogen atoms on the benzene ring.
Because of its methoxy group, this is the power supply radical, which can increase the electron cloud density of the benzene ring, making the electrophilic substitution reaction more likely to occur, and the substitution positions are mostly in the adjacent and para-position of the methoxy group. At the same time, the oxygen atom in the methoxy group has lone pair electr The
methyl group is also a donator group. Although the donator capacity is weaker than that of the methoxy group, it also affects the activity of the benzene ring, which increases the density of the adjacent and para-position electron clouds of the benzene ring, which is conducive to the attack of electrophilic reagents.
also contains a dioxy structure. If the dioxy is a peroxy structure, it is active and highly oxidizing, and is easy to decompose to produce free radicals, causing many chemical reactions. If it is an ordinary ether bond, the oxygen is relatively stable, but the carbon-oxygen bond of the ether bond can break under certain conditions, such as strong acid and high temperature.
Overall, 1% 2C2 + - + dioxy + - + 5 + - + methoxy + - + 3 + - + methylbenzene contains various functional groups and is rich in chemical properties. It may have important applications and reaction characteristics in the fields of organic synthesis and medicinal chemistry.
Because of its methoxy group, this is the power supply radical, which can increase the electron cloud density of the benzene ring, making the electrophilic substitution reaction more likely to occur, and the substitution positions are mostly in the adjacent and para-position of the methoxy group. At the same time, the oxygen atom in the methoxy group has lone pair electr The
methyl group is also a donator group. Although the donator capacity is weaker than that of the methoxy group, it also affects the activity of the benzene ring, which increases the density of the adjacent and para-position electron clouds of the benzene ring, which is conducive to the attack of electrophilic reagents.
also contains a dioxy structure. If the dioxy is a peroxy structure, it is active and highly oxidizing, and is easy to decompose to produce free radicals, causing many chemical reactions. If it is an ordinary ether bond, the oxygen is relatively stable, but the carbon-oxygen bond of the ether bond can break under certain conditions, such as strong acid and high temperature.
Overall, 1% 2C2 + - + dioxy + - + 5 + - + methoxy + - + 3 + - + methylbenzene contains various functional groups and is rich in chemical properties. It may have important applications and reaction characteristics in the fields of organic synthesis and medicinal chemistry.
What are the main uses of 1,2-dichloro-5-methoxy-3-methylbenzene?
1% 2C2-dioxy-5-methoxy-3-methylindole has important functions in many fields.
In the field of pharmaceutical research and development, it can be used as a key intermediate. Through specific chemical transformation, compounds with unique pharmacological activities can be derived. For example, in the development of drugs for the treatment of neurological diseases, this is used as a starting material to construct novel chemical structures through multi-step reactions, which may affect the regulation of neurotransmitters and provide a new direction for the creation of therapeutic drugs for Parkinson's, Alzheimer's and other diseases; in the development of cardiovascular drugs, by modifying the structure of this compound, innovative drugs that regulate vascular tone and improve cardiac function may be developed.
In the field of materials science, 1% 2C2-dioxy-5-methoxy-3-methylindole also has outstanding performance. Due to its unique chemical structure, it can be applied to organic optoelectronic devices due to its special photoelectric properties. For example, when preparing organic Light Emitting Diode (OLED), its rational introduction into the light-emitting layer material may optimize the luminous efficiency, color purity and stability of the device, and promote the display technology towards higher resolution, wider color gamut and lower energy consumption; in the field of solar cells, as a component of photosensitive materials, it may improve the capture and conversion efficiency of light energy, and help the development of high-efficiency solar cells.
In the dye industry, it can be used as a key raw material for the synthesis of new dyes. Due to its structural characteristics, it can produce specific colors and light absorption characteristics, and the synthesized dyes may show advantages in textile printing and dyeing, ink manufacturing, etc. If used in textile printing and dyeing, fabrics can show more vivid and lasting colors, and have good washing and light fastness; when used in ink manufacturing, it can bring clear and bright color performance to printed matter to meet high-end printing needs.
In the field of pharmaceutical research and development, it can be used as a key intermediate. Through specific chemical transformation, compounds with unique pharmacological activities can be derived. For example, in the development of drugs for the treatment of neurological diseases, this is used as a starting material to construct novel chemical structures through multi-step reactions, which may affect the regulation of neurotransmitters and provide a new direction for the creation of therapeutic drugs for Parkinson's, Alzheimer's and other diseases; in the development of cardiovascular drugs, by modifying the structure of this compound, innovative drugs that regulate vascular tone and improve cardiac function may be developed.
In the field of materials science, 1% 2C2-dioxy-5-methoxy-3-methylindole also has outstanding performance. Due to its unique chemical structure, it can be applied to organic optoelectronic devices due to its special photoelectric properties. For example, when preparing organic Light Emitting Diode (OLED), its rational introduction into the light-emitting layer material may optimize the luminous efficiency, color purity and stability of the device, and promote the display technology towards higher resolution, wider color gamut and lower energy consumption; in the field of solar cells, as a component of photosensitive materials, it may improve the capture and conversion efficiency of light energy, and help the development of high-efficiency solar cells.
In the dye industry, it can be used as a key raw material for the synthesis of new dyes. Due to its structural characteristics, it can produce specific colors and light absorption characteristics, and the synthesized dyes may show advantages in textile printing and dyeing, ink manufacturing, etc. If used in textile printing and dyeing, fabrics can show more vivid and lasting colors, and have good washing and light fastness; when used in ink manufacturing, it can bring clear and bright color performance to printed matter to meet high-end printing needs.
What are the synthesis methods of 1,2-dichloro-5-methoxy-3-methylbenzene?
To prepare 1-2-dichloro-5-methoxy-3-methylbenzene, there are various methods.
First, it can be started from suitable aromatic hydrocarbons. Select aromatic hydrocarbons with corresponding substituents, such as benzene derivatives containing methoxy and methyl, and perform chlorination reactions with chlorination reagents. Common chlorination reagents include chlorine gas, sulfoxide chloride, etc. Under suitable reaction conditions, such as specific temperature, pressure and catalyst existence, chlorine atoms can selectively replace hydrogen atoms at specific positions on the benzene ring. After precise control of the reaction process and conditions, the target product can be obtained.
Second, the method of gradually constructing substituents can be used. First, methoxy-containing benzene is used as the raw material, and methyl is introduced through a suitable alkylation reaction. The alkylation reagent can be methyl halide, etc. Then, the obtained product is chlorinated, and the reaction sequence and conditions are cleverly designed to introduce chlorine atoms according to the desired position, and finally 1-2-dichloro-5-methoxy-3-methylbenzene is obtained.
Third, or the reaction involving organometallic reagents can be considered. Using the coupling reaction of organometallic reagents and halogenated aromatics, etc., through rational design of synthesis routes, different substituents are introduced into the benzene ring in an orderly manner to achieve the purpose of synthesizing the target product. This process requires fine regulation of reaction conditions, such as reaction temperature, solvent, catalyst type and dosage, to ensure the high efficiency and selectivity of the reaction.
When synthesizing this compound, the conditions of each reaction step, the selection of reagents and the avoidance of side reactions need to be carefully considered. After many tests and optimizations, a satisfactory synthesis effect can be obtained.
First, it can be started from suitable aromatic hydrocarbons. Select aromatic hydrocarbons with corresponding substituents, such as benzene derivatives containing methoxy and methyl, and perform chlorination reactions with chlorination reagents. Common chlorination reagents include chlorine gas, sulfoxide chloride, etc. Under suitable reaction conditions, such as specific temperature, pressure and catalyst existence, chlorine atoms can selectively replace hydrogen atoms at specific positions on the benzene ring. After precise control of the reaction process and conditions, the target product can be obtained.
Second, the method of gradually constructing substituents can be used. First, methoxy-containing benzene is used as the raw material, and methyl is introduced through a suitable alkylation reaction. The alkylation reagent can be methyl halide, etc. Then, the obtained product is chlorinated, and the reaction sequence and conditions are cleverly designed to introduce chlorine atoms according to the desired position, and finally 1-2-dichloro-5-methoxy-3-methylbenzene is obtained.
Third, or the reaction involving organometallic reagents can be considered. Using the coupling reaction of organometallic reagents and halogenated aromatics, etc., through rational design of synthesis routes, different substituents are introduced into the benzene ring in an orderly manner to achieve the purpose of synthesizing the target product. This process requires fine regulation of reaction conditions, such as reaction temperature, solvent, catalyst type and dosage, to ensure the high efficiency and selectivity of the reaction.
When synthesizing this compound, the conditions of each reaction step, the selection of reagents and the avoidance of side reactions need to be carefully considered. After many tests and optimizations, a satisfactory synthesis effect can be obtained.
What are the precautions for using 1,2-dichloro-5-methoxy-3-methylbenzene?
1% 2C2-dioxy-5-methoxy-3-methylindole This substance requires many precautions during use.
First of all, due to its special chemical structure and properties, it is necessary to strictly follow the established procedures and safety guidelines when operating. When taking and handling, it is necessary to prepare suitable protective equipment, such as gloves, goggles and protective clothing, to prevent this substance from coming into direct contact with the skin and eyes and causing damage to the body.
Furthermore, this chemical substance may be toxic and dangerous to a certain extent. In terms of storage, choose a dry, cool and well-ventilated place, away from fire sources, heat sources and oxidants, etc., to guard against accidents such as fires and explosions. At the same time, it is necessary to properly isolate it from other chemicals to avoid mutual reactions and accidents.
In terms of the use environment, it is necessary to ensure that the ventilation conditions in the place are good to prevent the accumulation of volatile gaseous substances and endanger human health. If it is accidentally spilled during operation, emergency treatment measures should be initiated immediately. According to the characteristics of this substance, adsorption materials should be reasonably selected to clean it up to avoid its diffusion.
In addition, the amount of this substance used must be precisely controlled, and accurate measurement should be made according to the actual needs of experiment or production, so as to avoid waste and prevent adverse consequences caused by excessive use. After use, the residue should be properly disposed of in accordance with regulations and must not be discarded at will to avoid pollution to the environment.
In short, during the use of 1% 2C2-dioxy-5-methoxy-3-methylindole, safety awareness must be tight at all times, and all aspects of operation must be strictly regulated, so as to ensure the safety of personnel and the environment, and at the same time ensure the smooth achievement of the purpose of use.
First of all, due to its special chemical structure and properties, it is necessary to strictly follow the established procedures and safety guidelines when operating. When taking and handling, it is necessary to prepare suitable protective equipment, such as gloves, goggles and protective clothing, to prevent this substance from coming into direct contact with the skin and eyes and causing damage to the body.
Furthermore, this chemical substance may be toxic and dangerous to a certain extent. In terms of storage, choose a dry, cool and well-ventilated place, away from fire sources, heat sources and oxidants, etc., to guard against accidents such as fires and explosions. At the same time, it is necessary to properly isolate it from other chemicals to avoid mutual reactions and accidents.
In terms of the use environment, it is necessary to ensure that the ventilation conditions in the place are good to prevent the accumulation of volatile gaseous substances and endanger human health. If it is accidentally spilled during operation, emergency treatment measures should be initiated immediately. According to the characteristics of this substance, adsorption materials should be reasonably selected to clean it up to avoid its diffusion.
In addition, the amount of this substance used must be precisely controlled, and accurate measurement should be made according to the actual needs of experiment or production, so as to avoid waste and prevent adverse consequences caused by excessive use. After use, the residue should be properly disposed of in accordance with regulations and must not be discarded at will to avoid pollution to the environment.
In short, during the use of 1% 2C2-dioxy-5-methoxy-3-methylindole, safety awareness must be tight at all times, and all aspects of operation must be strictly regulated, so as to ensure the safety of personnel and the environment, and at the same time ensure the smooth achievement of the purpose of use.
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