1-Chloro-2-Methoxybenzene
Linshang Chemical
HS Code |
473734 |
Chemical Formula | C7H7ClO |
Molar Mass | 142.58 g/mol |
Appearance | Colorless to light yellow liquid |
Odor | Characteristic aromatic odor |
Density | 1.165 g/cm³ (at 20 °C) |
Boiling Point | 193 - 195 °C |
Melting Point | -25 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | 73 °C |
As an accredited 1-Chloro-2-Methoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 1 - chloro - 2 - methoxybenzene packaged in 500 - ml bottles, quantity: 10 bottles per case. |
Storage | 1 - Chloro - 2 - methoxybenzene should be stored in a cool, well - ventilated area, away from direct sunlight. It should be kept in a tightly sealed container to prevent vapor leakage. Store it separately from oxidizing agents, strong acids, and bases to avoid potential chemical reactions. The storage facility should comply with safety regulations for handling and storing flammable and potentially hazardous chemicals. |
Shipping | 1 - Chloro - 2 - methoxybenzene is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring proper handling to prevent spills and exposure during transit. |
Competitive 1-Chloro-2-Methoxybenzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 1-Chloro-2-Methoxybenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
First of all, the presence of chlorine atoms and methoxy groups in this compound endows it with specific reactivity. The chlorine atom is a halogen atom and has a tendency to nucleophilic substitution. Under suitable conditions for nucleophilic reagents and reactions, the chlorine atom can be replaced by a nucleophilic group. In case of hydroxyl negative ions (OH), a nucleophilic substitution reaction can occur, and the chlorine atom leaves, and the hydroxyl group replaces it to generate 2-methoxyphenol.
Furthermore, the methoxy group is the power supply radical, which can increase the electron cloud density of the benzene ring. This electronic effect makes the benzene ring more prone to electrophilic substitution. Taking the bromination reaction as an example, the electron cloud density of the adjacent and para-site of the methoxy group is relatively higher, and the bromine cation (Br 🥰) tends to attack the adjacent and para-site of the methoxy group to form the corresponding brominated product.
At the same time, in the molecule of 1-chloro-2-methoxybenzene, the conjugate system of the benzene ring makes it stable. However, under the action of strong oxidants, the benzene ring may also be oxidized. However, due to the influence of methoxy and chlorine atoms, the degree of difficulty of oxidation reaction is different from that of benzene.
In addition, the bond energy of carbon-chlorine bond and carbon-oxygen bond in this compound is different. Under the influence of heat, light and other conditions, the bond may be broken, triggering a series of chemical reactions. And its methoxy group may also participate in ether bond-related reactions. For example, under acidic conditions, the methoxy group may undergo protonation, which may lead to ether bond fracture.
In summary, 1-chloro-2-methoxybenzene exhibits rich and diverse chemical properties due to the existence of chlorine atoms and methoxy groups, and has important potential applications in organic synthesis and other fields.
First, it can be used as a raw material for organic synthesis. In the preparation of fine chemicals, it is a key intermediate. For example, in the synthesis of medicine, this is used as a starting material. Through a series of chemical reactions, molecular structures with specific pharmacological activities can be constructed. For example, in the synthesis of some antibacterial drugs, 1-chloro-2-methoxybenzene is involved, and through substitution, addition and other reactions, it gradually generates active pharmaceutical ingredients. In the synthesis of pesticides, it also plays an important role.
Second, it is also used in the fragrance industry. Due to its unique chemical structure, it can be properly converted to prepare fragrances with special aromas. The aroma emitted by its derivatives can be fresh and pleasant, or rich and mellow. It is used to prepare perfumes, air fresheners, detergents and other products, giving them a unique smell, enhancing product quality and market competitiveness.
Third, it has emerged in the field of materials science. Can be used as a monomer for synthesizing functional materials. Through polymerization, its structural units are introduced into the main chain or side chain of polymer materials, endowing the materials with special properties such as good solubility, thermal stability, and electrical properties, providing a foundation for the research and development of new materials. It has potential application value in electronic devices, optical materials, and so on.
The second method is to use o-chlorophenol as the starting material. O-chlorophenol reacts with methylating reagents, such as dimethyl sulfate or iodomethane, under alkaline conditions. Sodium hydroxide or potassium carbonate can be selected as the base. The reaction goes through a nucleophilic substitution process, and the hydrogen of phenolic hydroxyl is replaced by methoxy to obtain 1-chloro-2-methoxybenzene. This reaction also needs to be carried out in a suitable solvent to ensure full contact of the reactants and improve the reaction efficiency.
There are also those who use anisole as a raw material. The anisole is first halogenated under appropriate conditions. The halogenating reagent can be chlorine gas or N-chlorosuccinimide (NCS). 1-Chloro-2-methoxybenzene can be prepared by electrophilic substitution reaction on the aromatic ring and the introduction of chlorine atoms at a specific position in the benzene ring. In this process, the control of reaction conditions is very critical, such as reaction temperature, reagent dosage ratio, etc., all of which will affect the selectivity and yield of the product.
The above synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively weigh the availability of raw materials, the difficulty of controlling reaction conditions, product purity requirements, and cost to choose the most suitable method.
First, this substance has certain toxicity and irritation, so the storage place should be well ventilated and away from fire and heat sources to avoid its decomposition by heat and release toxic hydrogen chloride and other gases. If it is heated or causes the internal pressure of the container to rise, there is a risk of cracking and explosion.
Second, because it is an organic halide, it may be harmful to the environment, and it should be prevented from leaking during storage. If it leaks, the halide will enter the soil, water body, or pollute the environment. When transporting, also ensure that the packaging is intact to prevent leakage during transportation. The packaging must be sturdy and able to withstand the vibration, collision and extrusion of normal transportation.
Third, 1-chloro-2-methoxybenzene is flammable in case of open flames and hot topics. Transportation vehicles should be equipped with fire extinguishers, and drivers and escorts must be familiar with the characteristics of this material and emergency handling methods. In the storage warehouse, suitable containment materials and fire extinguishing equipment should also be prepared for emergency use in case of leakage or fire.
Fourth, the storage temperature should be controlled within an appropriate range. If the temperature is too high, it may accelerate its volatilization and reaction; if the temperature is too low, it may solidify and affect access. And should be stored separately from oxidizing agents, acids, alkalis, etc., to avoid their mutual reaction.
Fifth, in the storage and transportation place, there should be obvious warning signs, so that relevant personnel are aware of the danger of this thing. Operators should also wear appropriate protective equipment, such as gas masks, protective gloves, etc., to prevent contact with the human body and ensure personal safety.
At the environmental level, if it is released into nature, it can cause pollution to water bodies, soil and atmosphere. In water bodies, it may affect the survival and reproduction of aquatic organisms. Many aquatic organisms are extremely sensitive to chemicals in water. The presence of 1-chloro-2-methoxybenzene may interfere with their normal physiological functions, causing their growth to be blocked, reproductive capacity to decline, and even death, thereby destroying the balance of aquatic ecosystems. In soil, it may change the physical and chemical properties of soil, affect the activity and community structure of soil microorganisms, hinder the absorption of nutrients by plant roots, and have adverse effects on vegetation growth and development. Once it enters the atmosphere, it may participate in photochemical reactions, generating more harmful pollutants, affecting air quality, and may also have potential effects on regional climate.
As far as human health is concerned, 1-chloro-2-methoxybenzene has certain toxicity. Inhaled through the respiratory tract, it can irritate the mucosa of the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure to this environment may increase the risk of respiratory diseases. If exposed through skin, it may enter the human body through the skin barrier, causing adverse reactions such as skin allergies, redness, swelling, and itching. If ingested by mistake, it may damage the digestive system, causing nausea, vomiting, abdominal pain, and other symptoms. In severe cases, it will be life-threatening. And some of these organic compounds may have potential carcinogenicity, teratogenicity and mutagenicity, long-term exposure or damage to human genetic material, increase the risk of cancer, and may also have adverse effects on fetal development.
Therefore, in the production, use and disposal of 1-chloro-2-methoxybenzene, proper protective measures and environmental protection measures must be taken to reduce its harm to the environment and human health.
Let's talk about the nucleophilic substitution reaction first. Because of its high activity of chlorine atoms on the benzene ring, it is vulnerable to attack by nucleophilic reagents. For example, in an aqueous solution of sodium hydroxide, the chlorine atom may be replaced by a hydroxyl group to generate 2-methoxyphenol. In this reaction, the hydroxyl negative ion acts as a nucleophilic reagent. By virtue of its own electron-rich properties, it attacks the carbon atom attached to the chlorine atom, and the chloride ion leaves, and the reaction is completed.
Say electrophilic substitution Methoxy is an electron donor group, which can increase the electron cloud density of the benzene ring, especially the ortho and para-position. Therefore, electrophilic reagents are prone to attack the ortho and para-position of methoxy groups. If brominated with bromine, the main product is 4-bromo-1-chloro-2-methoxybenzene. Bromine cations, as electrophilic reagents, prefer to attack high electron cloud densities. The conjugation effect of methoxy groups makes the ortho and para-position electron clouds more dense than the meta-position, so the ortho and para-position products are mostly.
In addition, 1-chloro-2-methoxybenzene can also participate in metal catalytic reactions. Under the catalysis of palladium, it can be coupled with boron-containing compounds to form new carbon-carbon bonds. This reaction is widely used in the field of organic synthesis and can be used to prepare complex organic molecules.
At the same time, because there are both chlorine atoms and methoxy groups in the molecule, the two functional groups interact with each other, resulting in the complex and rich chemical properties of the compound. In the field of organic synthesis chemistry, it is a key intermediate, and many organic compounds with unique properties and uses can be derived through different chemical reactions.
First, in the field of synthesis, this compound plays an important role. It is often used as an important medium in the synthesis of polymers. Due to the characteristics of its molecules, it can be reacted by a specific reaction, introduced into other functionalities, and produced. For example, in some of the synthesis pathways of pain and solution, 1-chloro-2-methoxybenzene can be used as a starting material to generate polymers with chemical activity.
Second, it is also important in manufacturing. It can be used to synthesize multiple compounds, such as herbicides, weeds, etc. Its chemical properties enable it to react to other compounds and generate chemical components with specific biological activities, which are used to prevent and control diseases and diseases of crops and ensure the good harvest.
In addition, in the fragrance industry, 1-chloro-2-methoxybenzene also has a place. Because it can provide special fragrance ingredients, it can be used as a raw material for fragrance synthesis. It is used for blending various flavors, adding fragrance characteristics to products, and is widely used in perfumes, toiletries, etc.
In addition, in the research of synthetic chemicals, this compound is often used as a model substrate. Due to its comprehensive and representative nature, researchers can explore new synthesis methods, reverse mechanisms, etc. by conducting various chemical and anti-chemical studies, and promote the development of synthetic synthesis. Therefore, 1-chloro-2-methoxybenzene has important value in the field of industrial and biological chemical research due to its various uses.
There is also a method of preparing 1-chloro-2-methoxybenzene by methylation from o-chlorophenol. Methylation reagents such as dimethyl sulfate and iodomethane are commonly used. Taking dimethyl sulfate as an example, the reaction needs to be carried out under alkaline conditions, and the base can be selected from sodium hydroxide, potassium carbonate, etc. The alkaline environment is conducive to the deprotonation of phenolic hydroxyl groups and enhances their nucleophilicity, so as to undergo nucleophilic substitution with dimethyl sulfate. During the reaction process, close attention should be paid to the control of temperature and the ratio of reactants to prevent the formation of polymethylated products.
In addition, palladium-catalyzed cross-coupling reactions have also been used to prepare 1-chloro-2-methoxylbenzene. For example, a suitable halogenated aromatic hydrocarbon reacts with methoxylation reagents in the presence of palladium catalysts and ligands. This method can achieve precise functionalization and high reaction selectivity. However, palladium catalysts are expensive, demanding reaction conditions, require an anhydrous and anaerobic environment, and the reaction time is long, which is expensive in actual production, limiting their large-scale application.
All of the above synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider various factors such as the availability of raw materials, the difficulty of controlling reaction conditions, production cost and product purity, and choose the optimal method.
When storing it, the first thing to do is to choose a cool and ventilated warehouse. This compound is easy to decompose when heated, and the high temperature environment may cause danger. Therefore, the temperature of the warehouse should be controlled within a reasonable range, and it must not be too high. The humidity of the warehouse should also be paid attention to. If the humidity is too high, it may affect its stability and cause deterioration.
Furthermore, when storing, it must be stored separately from oxidants, acids, bases, etc., and must not be mixed. Due to its active chemical properties, contact with the above substances may cause severe chemical reactions, such as combustion, explosion and other serious consequences.
And the storage area should be equipped with suitable materials to contain leaks. In the event of a leak, it can be dealt with in a timely and effective manner to prevent the spread of pollution and reduce hazards.
During transportation, the packaging must be tight. Make sure that the transportation container is intact and well sealed to avoid leakage of 1-chloro-2-methoxybenzene. The selected transportation container must be adapted to the characteristics of the substance, capable of withstanding its corrosion, and ensuring transportation safety.
Transportation vehicles must also meet relevant safety standards and be equipped with necessary emergency treatment equipment and protective supplies. Such as fire extinguishers, leakage emergency treatment tools, etc., to prepare for emergencies. Transportation personnel must undergo professional training and be familiar with the characteristics and emergency treatment methods of 1-chloro-2-methoxybenzene. During transportation, traffic rules and transportation regulations should be strictly followed to avoid bumps and vibrations to prevent package damage and leakage.
In short, the storage and transportation of 1-chloro-2-methoxybenzene requires all-round prudent treatment to ensure the safety of personnel and the environment is not polluted.
Discussing the impact on the environment, if this compound is released in nature, it may be difficult to degrade. Its accumulation in the soil can disturb the soil ecology and cause changes in the structure and function of the soil microbial community. Entering the water body endangers aquatic organisms. Or cause poisoning of fish, plankton, etc., damage their growth and reproduction ability, and then disrupt the aquatic ecological balance. And it is volatile. After entering the atmosphere, it may participate in photochemical reactions, disturb the atmospheric environment, and increase the possibility of bad weather such as smog.
As for the impact on human health, the harm should not be underestimated. People can get sick if they ingest this compound through breathing, skin contact or diet. It enters the body through the respiratory tract, or irritates the mucosa of the respiratory tract, causing cough, asthma and other diseases. Skin contact can cause contact dermatitis, showing redness, swelling and itching. If taken by mistake, it may damage the digestive system, causing nausea, vomiting and abdominal pain. In particular, long-term exposure to this substance may cause cancer. Because studies have shown that some halogenated aromatic compounds are potentially carcinogenic, 1-chloro-2-methoxybenzene is also such, so it must be prevented. In short, 1-chloro-2-methoxybenzene is harmful to the environment and human health. It should be handled with caution to prevent it from polluting the environment and protecting people's health.

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