Linshang Chemical
PRODUCTS
Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci)
Linshang Chemical
|
HS Code |
537883 |
| Chemical Formula | C7H6ClNO2 |
| Molar Mass | 171.58 g/mol |
| Appearance | Solid (usually) |
| Melting Point | Data needed |
| Boiling Point | Data needed |
| Density | Data needed |
| Solubility In Water | Low solubility (organic compound) |
| Solubility In Organic Solvents | Soluble in common organic solvents |
| Odor | Typical aromatic odor (guess based on structure) |
| Flammability | Combustible |
| Stability | Stable under normal conditions, but reactive with strong oxidizers |
As an accredited Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottle of 1 - chloro - 3 - methyl - 4 - nitro - benzene (9CI) for chemical use. |
| Storage | 1 - Chloro - 3 - methyl - 4 - nitrobenzene (9CI) should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points. It should be stored in a tightly sealed container, preferably made of corrosion - resistant materials like stainless steel or certain plastics. Keep it separated from oxidizing agents, reducing agents, and substances that could react with it, to prevent potential chemical reactions and ensure safety. |
| Shipping | The chemical "Benzene, 1 - chloro - 3 - methyl - 4 - nitro - (9ci)" must be shipped in accordance with strict hazardous materials regulations. Use appropriate, labeled containers to prevent leakage during transit. |
Competitive Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci) 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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci) in China?
As a trusted Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci) manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading Benzene, 1-Chloro-3-Methyl-4-Nitro- (9Ci) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the chemical properties of 1-chloro-3-methyl-4-nitrobenzene (9ci)?
This is an organic compound named 1-bromo-3-methyl-4-tert-butylbenzene (9ci). Looking at the structure of this compound, the bromine atom, methyl and tert-butyl are all connected to the benzene ring.
Its chemical properties are as follows:
The benzene ring is aromatic and quite stable, and common reactions such as electrophilic substitution reactions. Because the electron cloud density on the benzene ring is relatively high, it is vulnerable to electrophilic attack. In this compound, the bromine atom is an electron-withdrawing group, and the methyl and tert-butyl groups are the power supply groups. The electron cloud density of the benzene ring can be increased by the donating radical, and the reaction is more likely to occur in the electrophilic substitution reaction, and mainly occurs in the ortho and para-position; while the electron-absorbing action of the bromine atom will reduce the electron cloud density of the benzene ring, and the electrophilic substitution reaction activity will be slightly reduced.
Both methyl and tert-butyl are alkyl, with certain properties of saturated hydrocarbons. Alkyl groups can undergo free radical substitution reactions. For example, under light or high temperature conditions, they can react with halogen elements, and hydrogen atoms are replaced by halogen atoms.
Bromine atoms can undergo various reactions. One is the nucleophilic substitution reaction. Under suitable conditions for nucleophilic reagents and reactions, bromine atoms can be replaced by other nucleophilic groups, such as co-heating with sodium hydroxide aqueous solution, bromine atoms can be replaced by hydroxyl groups to form corresponding phenolic compounds; when reacted with sodium alcohol, ether compounds can be formed. The second is the elimination reaction. Under the action of a strong base, a elimination reaction can occur to form compounds containing carbon-carbon double bonds.
In summary, 1-bromo-3-methyl-4-tert-butylbenzene (9ci) exhibits rich chemical properties due to the characteristics of functional groups and phenyl rings, and has important application value in the field of organic synthesis.
Its chemical properties are as follows:
The benzene ring is aromatic and quite stable, and common reactions such as electrophilic substitution reactions. Because the electron cloud density on the benzene ring is relatively high, it is vulnerable to electrophilic attack. In this compound, the bromine atom is an electron-withdrawing group, and the methyl and tert-butyl groups are the power supply groups. The electron cloud density of the benzene ring can be increased by the donating radical, and the reaction is more likely to occur in the electrophilic substitution reaction, and mainly occurs in the ortho and para-position; while the electron-absorbing action of the bromine atom will reduce the electron cloud density of the benzene ring, and the electrophilic substitution reaction activity will be slightly reduced.
Both methyl and tert-butyl are alkyl, with certain properties of saturated hydrocarbons. Alkyl groups can undergo free radical substitution reactions. For example, under light or high temperature conditions, they can react with halogen elements, and hydrogen atoms are replaced by halogen atoms.
Bromine atoms can undergo various reactions. One is the nucleophilic substitution reaction. Under suitable conditions for nucleophilic reagents and reactions, bromine atoms can be replaced by other nucleophilic groups, such as co-heating with sodium hydroxide aqueous solution, bromine atoms can be replaced by hydroxyl groups to form corresponding phenolic compounds; when reacted with sodium alcohol, ether compounds can be formed. The second is the elimination reaction. Under the action of a strong base, a elimination reaction can occur to form compounds containing carbon-carbon double bonds.
In summary, 1-bromo-3-methyl-4-tert-butylbenzene (9ci) exhibits rich chemical properties due to the characteristics of functional groups and phenyl rings, and has important application value in the field of organic synthesis.
What are the physical properties of 1-chloro-3-methyl-4-nitrobenzene (9ci)
1 + -Deuterium-3-methyl-4-tert-butyl naphthalene (9ci) is one of the organic compounds. Its physical properties are many, and let me tell them one by one.
When it comes to appearance, this compound is often in a solid state, and its specific color may vary slightly due to factors such as purity and crystal form, or it is white or slightly yellowish, but it is usually pure and light.
Looking at its melting point, this is one of the important physical properties for the identification and study of this compound. After many experiments, its melting point is in a specific temperature range, and this temperature value plays a key role in guiding the physical state transition of the compound under different conditions. The boiling point of
is also its significant physical property. When the external pressure reaches a certain standard, the compound will change from liquid to gaseous state. This boiling point value is related to its application in chemical operations such as distillation and separation, and is of great significance to industrial production and scientific research.
In terms of solubility, this compound has different properties in common organic solvents. In non-polar organic solvents, such as toluene and n-hexane, it has good solubility and can be evenly dispersed to form a uniform and stable solution. However, in polar solvents, such as water, the solubility is very poor. Due to the characteristics of molecular structure, the force between water molecules is weak and it is difficult to miscible.
Density is also a physical property that cannot be ignored. Under specific temperature and pressure conditions, its density has a fixed value, which is of great significance for accurate measurement, storage and transportation of the compound, and is related to the measurement and container selection in actual operation.
In addition, the refractive index of the compound also has a specific value. The refractive index reflects its ability to refract light. It is an important reference index in the field of optical materials and analysis and detection, and can be used for purity analysis and compound identification.
The above are the main physical properties of 1 + -deuterium-3-methyl-4-tert-butyl naphthalene (9ci), which are related to each other and together build a knowledge of the physical aspects of the compound. It is of great value in many fields such as scientific research and production.
When it comes to appearance, this compound is often in a solid state, and its specific color may vary slightly due to factors such as purity and crystal form, or it is white or slightly yellowish, but it is usually pure and light.
Looking at its melting point, this is one of the important physical properties for the identification and study of this compound. After many experiments, its melting point is in a specific temperature range, and this temperature value plays a key role in guiding the physical state transition of the compound under different conditions. The boiling point of
is also its significant physical property. When the external pressure reaches a certain standard, the compound will change from liquid to gaseous state. This boiling point value is related to its application in chemical operations such as distillation and separation, and is of great significance to industrial production and scientific research.
In terms of solubility, this compound has different properties in common organic solvents. In non-polar organic solvents, such as toluene and n-hexane, it has good solubility and can be evenly dispersed to form a uniform and stable solution. However, in polar solvents, such as water, the solubility is very poor. Due to the characteristics of molecular structure, the force between water molecules is weak and it is difficult to miscible.
Density is also a physical property that cannot be ignored. Under specific temperature and pressure conditions, its density has a fixed value, which is of great significance for accurate measurement, storage and transportation of the compound, and is related to the measurement and container selection in actual operation.
In addition, the refractive index of the compound also has a specific value. The refractive index reflects its ability to refract light. It is an important reference index in the field of optical materials and analysis and detection, and can be used for purity analysis and compound identification.
The above are the main physical properties of 1 + -deuterium-3-methyl-4-tert-butyl naphthalene (9ci), which are related to each other and together build a knowledge of the physical aspects of the compound. It is of great value in many fields such as scientific research and production.
What is the main use of 1-chloro-3-methyl-4-nitrobenzene (9ci)?
9Ci refers to 1-tritium-3-methyl-4-carbonyl indole, which has important uses. In the field of medicine, it can be used as a key intermediate for the synthesis of a variety of drugs. Because of its unique chemical structure, it can participate in specific chemical reactions to construct drug molecular structures with biological activity. For example, in the development of some anti-tumor drugs, its structural characteristics can be used to combine with other chemical groups to design drugs that can precisely act on tumor cell targets, interfere with tumor cell growth and proliferation-related signaling pathways, and thus exert anti-cancer effects.
It is also valuable in materials science. It can be used as a synthetic raw material for functional materials, giving materials special properties. For example, in the synthesis of organic optoelectronic materials, introducing them into the molecular structure of materials can change the photoelectric properties of materials, making them exhibit better photoelectric conversion efficiency and stability in optoelectronic devices such as organic Light Emitting Diodes (OLEDs), solar cells, etc., and expand the application range of materials in the field of optoelectronics.
At the same time, in organic synthetic chemistry, it is an important synthetic building block. Chemists can perform derivatization reactions according to their structures, and prepare a series of organic compounds with diverse structures by modifying different substituents. This provides a rich material basis for the development of organic synthetic chemistry, promotes the progress of organic synthesis methodologies, and helps to develop more novel and efficient organic synthesis routes.
It is also valuable in materials science. It can be used as a synthetic raw material for functional materials, giving materials special properties. For example, in the synthesis of organic optoelectronic materials, introducing them into the molecular structure of materials can change the photoelectric properties of materials, making them exhibit better photoelectric conversion efficiency and stability in optoelectronic devices such as organic Light Emitting Diodes (OLEDs), solar cells, etc., and expand the application range of materials in the field of optoelectronics.
At the same time, in organic synthetic chemistry, it is an important synthetic building block. Chemists can perform derivatization reactions according to their structures, and prepare a series of organic compounds with diverse structures by modifying different substituents. This provides a rich material basis for the development of organic synthetic chemistry, promotes the progress of organic synthesis methodologies, and helps to develop more novel and efficient organic synthesis routes.
What is the synthesis method of 1-chloro-3-methyl-4-nitrobenzene (9ci)?
To prepare 1-bromo-3-methyl-4-tert-butylbenzene (9ci), the following ancient method can be used.
First take m-methyl phenol, use tert-butyl chloride as a reagent, and carry out the Fu-gram alkylation reaction under the catalysis of anhydrous aluminum trichloride. This reaction is carried out at an appropriate temperature and in an inert gas-protected environment. Tert-butyl chloride attacks the m-methylphenol phenol ring to obtain 3-methyl-4-tert-butylphenol. The reason is that both phenolic hydroxyl and methyl are ortho-para-sites, and the phenolic hydroxyl localization effect is stronger, so tert-butyl mainly enters the phenolic hydroxyl para-site.
Then, take the prepared 3-methyl-4-tert-butylphenol, use a brominating agent such as liquid bromine, and carry out the bromination reaction in a suitable solvent such as dichloromethane at low temperature and in the presence of a catalyst such as iron powder. At this time, the phenolic hydroxyl group is a strongly activating group, which guides the bromine atom into the phenolic hydroxyl ortho-site, and then obtains 1-bromo-3-methyl-4-tert-butylbenzene. Because the phenolic hydroxyl group has a significant effect on the electron cloud density of the phenyl ring ortho-site, the ortho-site is more prone to electrophilic substitution.
Another feasible method is to first use m-methyl benzene to react with tert-butyl chloride and anhydrous aluminum trichloride to complete Fu-gram alkylation to obtain 3-methyl-tert-butyl benzene. Then use iron bromide as a catalyst to react with bromine elemental substance and perform bromination reaction. Because methyl is an ortho-para-site group, 1-bromo-3-methyl-4-tert-butyl benzene can be prepared. This process requires attention to the control of reaction conditions to ensure that the reaction proceeds smoothly in the expected direction to obtain a higher yield of the target product.
First take m-methyl phenol, use tert-butyl chloride as a reagent, and carry out the Fu-gram alkylation reaction under the catalysis of anhydrous aluminum trichloride. This reaction is carried out at an appropriate temperature and in an inert gas-protected environment. Tert-butyl chloride attacks the m-methylphenol phenol ring to obtain 3-methyl-4-tert-butylphenol. The reason is that both phenolic hydroxyl and methyl are ortho-para-sites, and the phenolic hydroxyl localization effect is stronger, so tert-butyl mainly enters the phenolic hydroxyl para-site.
Then, take the prepared 3-methyl-4-tert-butylphenol, use a brominating agent such as liquid bromine, and carry out the bromination reaction in a suitable solvent such as dichloromethane at low temperature and in the presence of a catalyst such as iron powder. At this time, the phenolic hydroxyl group is a strongly activating group, which guides the bromine atom into the phenolic hydroxyl ortho-site, and then obtains 1-bromo-3-methyl-4-tert-butylbenzene. Because the phenolic hydroxyl group has a significant effect on the electron cloud density of the phenyl ring ortho-site, the ortho-site is more prone to electrophilic substitution.
Another feasible method is to first use m-methyl benzene to react with tert-butyl chloride and anhydrous aluminum trichloride to complete Fu-gram alkylation to obtain 3-methyl-tert-butyl benzene. Then use iron bromide as a catalyst to react with bromine elemental substance and perform bromination reaction. Because methyl is an ortho-para-site group, 1-bromo-3-methyl-4-tert-butyl benzene can be prepared. This process requires attention to the control of reaction conditions to ensure that the reaction proceeds smoothly in the expected direction to obtain a higher yield of the target product.
Precautions for storage and transportation of 1-chloro-3-methyl-4-nitrobenzene (9ci)
When storing and transporting 1 + -deuterium-3-methyl-4-propylheptane (9ci), many points need to be paid attention to.
When storing, the first environment. This substance should be placed in a cool and ventilated place, away from fire and heat sources. Because of its certain volatility and flammability, high temperature and open flame can easily cause danger. The temperature of the warehouse should be strictly controlled, not too high, to prevent the material from evaporating and forming a flammable and explosive mixed gas. Humidity cannot be ignored, too humid environment or cause material deterioration, which affects its quality and stability.
Furthermore, the choice of container is very important. Containers that can be sealed should be used to prevent substances from evaporating and escaping, polluting the environment, and avoiding excessive contact with air, oxidation and other reactions. The material of the container used should not react chemically with the substance, such as some metal materials or react with some chemical substances, so it is necessary to choose suitable materials, such as specific plastic or glass materials.
When transporting, safety measures must be comprehensive. Vehicles must be equipped with fire and explosion-proof devices to prevent accidental open flames or static electricity during transportation, which may cause danger. Drivers and escorts should be professionally trained and familiar with the characteristics of the substance and emergency treatment methods. During transportation, route planning is also important. It is also important to avoid densely populated areas and busy traffic sections to reduce the possible harm caused by accidents.
The loading and unloading process also requires caution. It should be handled with care to avoid container collision, damage, and material leakage. In the event of a leak, the on-site personnel need to take immediate emergency measures, evacuate the surrounding people, seal the scene, and use appropriate methods to clean up and dispose of the material according to its characteristics. Do not panic.
When storing, the first environment. This substance should be placed in a cool and ventilated place, away from fire and heat sources. Because of its certain volatility and flammability, high temperature and open flame can easily cause danger. The temperature of the warehouse should be strictly controlled, not too high, to prevent the material from evaporating and forming a flammable and explosive mixed gas. Humidity cannot be ignored, too humid environment or cause material deterioration, which affects its quality and stability.
Furthermore, the choice of container is very important. Containers that can be sealed should be used to prevent substances from evaporating and escaping, polluting the environment, and avoiding excessive contact with air, oxidation and other reactions. The material of the container used should not react chemically with the substance, such as some metal materials or react with some chemical substances, so it is necessary to choose suitable materials, such as specific plastic or glass materials.
When transporting, safety measures must be comprehensive. Vehicles must be equipped with fire and explosion-proof devices to prevent accidental open flames or static electricity during transportation, which may cause danger. Drivers and escorts should be professionally trained and familiar with the characteristics of the substance and emergency treatment methods. During transportation, route planning is also important. It is also important to avoid densely populated areas and busy traffic sections to reduce the possible harm caused by accidents.
The loading and unloading process also requires caution. It should be handled with care to avoid container collision, damage, and material leakage. In the event of a leak, the on-site personnel need to take immediate emergency measures, evacuate the surrounding people, seal the scene, and use appropriate methods to clean up and dispose of the material according to its characteristics. Do not panic.
Scan to WhatsApp
