3 3 Methoxyphenyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-(3-Methoxyphenyl)pyridine

    Specifications

    HS Code

    836622

    Chemical Formula C12H11NO
    Molar Mass 185.22 g/mol
    Appearance Solid (usually)
    Melting Point Data needed
    Boiling Point Data needed
    Solubility Solubility data in different solvents needed
    Density Data needed
    Pka Data needed
    Logp Data needed
    Flash Point Data needed

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    General Information
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    Frequently Asked Questions

    As a leading 3-(3-Methoxyphenyl)pyridine 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 main uses of 3- (3-methoxyphenyl) pyridine?
    The main use of 3- (3-methoxybenzyl) is in the field of organic synthesis. Among many organic synthesis reactions, this group exhibits a unique role.
    First, in pharmaceutical chemical synthesis, it is often used as a protective group. For example, when reacting some pharmaceutical intermediates with polyfunctional groups, in order to avoid unnecessary reactions of hydroxyl groups at specific positions during the reaction, 3- (3-methoxybenzyl) can be introduced to protect them. After other reaction steps are completed, the protective group is removed through specific deprotection conditions, thereby retaining the original structure and activity of the target product. This method can precisely regulate the reaction check point, improve the selectivity of the reaction and the purity of the product, which is of great significance to the development and production of drugs.
    Second, in the total synthesis of complex natural products, 3- (3-methoxybenzyl) often acts as a key structural fragment. Many natural products have complex molecular structures, rich in diverse functional groups and special carbon skeletons. The introduction of 3- (3-methoxybenzyl) can help to construct specific carbon-carbon bonds or carbon-heteroatomic bonds, and realize the gradual construction of the molecular skeleton of natural products. With its unique electronic effect and steric resistance, it can guide the reaction in the desired direction, laying the foundation for the successful synthesis of natural products.
    Third, this group is also used in organic synthesis related to materials science. The preparation of some functional organic materials requires careful design and modification of molecular structures. The presence of 3- (3-methoxybenzyl) can change the electron cloud distribution, solubility and other physical and chemical properties of the material, thereby endowing the material with specific optical and electrical properties, etc., to meet the special needs of different fields for material properties.
    What are the physical properties of 3- (3-methoxyphenyl) pyridine?
    3 - (3 -methoxybenzyl) The physical properties of this substance are as follows:
    Its external properties are usually solid or liquid, with a specific melting temperature. If it is solid, the melting temperature is high and low, and the molecular force is low. Molecular force, high energy is required to break the lattice, so that the solid is melted, and the melting temperature will be high; vice versa. If it is liquid, the boiling rate also depends on the molecular force. The force is high, and the energy required to overcome the attractive force of the molecule is high, and the boiling phase is high.
    In terms of solubility, it depends on the different solubility. Due to the principle of similarity and phase solubility, if the molecule is soluble, it is easily soluble in the soluble solution, such as ethanol, water, etc.; if the molecule is not soluble, it is soluble in the non-soluble solution, such as benzene, carbon tetrachloride, etc.
    Density is also an important physical property, and its value reflects the density of the molecule. The density of the molecule and the density of the molecular arrangement vary. The molecular weight is large and the arrangement is dense, and the density of the phase is large.
    In addition, it may have a specific refractive index. The refractive index can reflect the degree of change in the direction of the light passing through the object. The molecular weight and phase formation of the substance can be used to determine this substance or its density.
    What are the synthesis methods of 3- (3-methoxyphenyl) pyridine?
    To prepare 3 - (3 - methoxybenzyl) acetone, there are various ways to synthesize it. First, it can be prepared by the condensation reaction of 3 - methoxybenzaldehyde and acetone. First, 3 - methoxybenzaldehyde and acetone are placed in a suitable reaction vessel, an appropriate amount of base is added as a catalyst, such as sodium hydroxide or potassium hydroxide, and the reaction is stirred at an appropriate temperature. This condensation reaction can cause condensation between the two molecules, eliminate a molecule of water, and obtain an intermediate product. Subsequent reduction steps, such as treatment with reducing agents such as sodium borohydride or lithium aluminum hydride, reduce the unsaturated bond of the intermediate product to obtain 3 - (3 - methoxybenzyl) acetone. < Br >
    Second, it can start from 3-methoxybenzyl chloride. First, 3-methoxybenzyl chloride is reacted with magnesium chips to make Grignard's reagent. Grignard's reagent is quite active, and then it reacts with acetone. The carbon-magnesium bond in Grignard's reagent is broken, and the carbon negative ion attacks the carbonyl carbon of acetone to form a new carbon-carbon bond. After the reaction is completed, the oxygen atom is protonated after acidification treatment, and the target product 3 - (3-methoxybenzyl) acetone can be obtained.
    Third, 3-methoxybenzoic acid is used as the starting material. First, it is converted into 3-methoxybenzoyl chloride, which can be reacted with thionyl chloride. Then 3-methoxybenzoyl chloride and acetone are acylated in the presence of a strong base to generate 3- (3-methoxybenzoyl) acetone. After that, the carbonyl oxygen is removed by the reduction step, and 3- (3-methoxybenzyl) acetone can also be obtained.
    These several synthesis methods have their own advantages and disadvantages, and they need to be selected according to the actual situation, such as the availability of raw materials, the difficulty of reaction conditions, and the purity requirements of the product.
    What are the precautions for using 3- (3-methoxyphenyl) pyridine?
    3 - (3 -methoxybenzyl) During use, the following items should be paid attention to:
    First, it concerns its chemical properties. This substance has specific chemical activity and reaction characteristics, and the corresponding rules of relevant chemical properties must be known and followed when storing and handling. For example, due to the presence of methoxy groups, or the unique activity and selectivity of certain chemical reactions, when operating, it is necessary to pay attention to the possibility of reaction with other reagents, so as not to cause unexpected reactions, which may lead to dangerous conditions or impure products.
    Second, safety protection. Appropriate protective equipment should be configured according to its chemical properties. If it is potentially irritating to the skin and eyes, wear protective gloves, goggles, etc. during operation to prevent direct contact with it. In addition, if the substance may evaporate harmful gases under specific conditions, the operating environment should be well ventilated, or even equipped with special ventilation facilities to avoid damage to the human body caused by the accumulation of harmful gases.
    Third, storage conditions cannot be ignored. It is necessary to choose an appropriate storage environment according to its stability requirements. If the substance is sensitive to light and heat, it should be stored in a cool and dark place, and attention should be paid to the material of the storage container to avoid chemical reactions with the container, which will affect its quality and performance.
    Fourth, access and operation specifications are very critical. During the operation, it is necessary to strictly follow the established operating procedures. Take an appropriate amount of the substance to avoid waste and unnecessary risks. In the mixing, heating and other operations, the reaction conditions, such as temperature, time, and the proportion of reactants, should be precisely controlled to ensure that the reaction can proceed smoothly as expected, obtain the ideal product, and prevent the occurrence of safety accidents due to improper operation.
    What is the market outlook for 3- (3-methoxyphenyl) pyridine?
    There are currently 3- (3-methoxybenzyl) products, and their market prospects are as follows:
    This 3- (3-methoxybenzyl) has potential in many fields. In the field of medicinal chemistry, methoxybenzyl structures are often key active fragments, and many drug development depends on them. If 3- (3-methoxybenzyl) can be used to synthesize new drugs or can be used for the treatment of specific diseases, the market is in constant demand for innovative drugs. If the research and development goes well, it will definitely occupy a place in the pharmaceutical market.
    In materials science, compounds containing such structures may endow materials with special properties. For example, materials with special optical, electrical or mechanical properties can be prepared. With the development of science and technology, the demand for special performance materials is increasing day by day. If relevant high-performance materials can be developed, there is also broad space for them in the electronic, optical materials and other markets.
    However, the market also has challenges. The synthesis process may be complex, and if the synthesis cost is too high, it will limit its large-scale production and marketing activities. And the market competition is fierce. Similar or alternative products may already exist in the market. To stand out, it needs to have significant advantages in performance and cost. Overall, the 3- (3-methoxybenzyl) market has a promising future, but it is necessary to overcome the difficulties of synthesis cost and competition. If it can be properly resolved, it will be able to achieve good development in the relevant market.