4 Pyridinemethanol 3 5 Dichloro Methyl
pyridine pyrrole pyrazine piperidine piperazine

4-pyridinemethanol, 3,5-dichloro-methyl-

    Specifications

    HS Code

    718693

    Chemical Formula C7H5Cl2NO
    Molecular Weight 190.027
    Appearance Solid (predicted)
    Boiling Point 324.3°C at 760 mmHg (predicted)
    Melting Point N/A
    Density 1.456 g/cm³ (predicted)
    Flash Point 149.9°C (predicted)
    Solubility In Water Insoluble (predicted)
    Logp 2.63 (predicted)
    Vapor Pressure 4.63E-05 mmHg at 25°C (predicted)

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    General Information
    Where to Buy 4-pyridinemethanol, 3,5-dichloro-methyl- in China?
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    Frequently Asked Questions

    As a leading 4-pyridinemethanol, 3,5-dichloro-methyl- 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 4-pyridinemethanol, 3,5-dichloro-methyl-?
    The chemical properties of 4-pyridine methanol, 3,5-dichloro-methyl-this substance are quite unique. In its structure, the pyridine ring has certain aromatic and basic properties, because the nitrogen atom of the pyridine ring has lone pairs of electrons and can accept protons.
    In chemical reactions, the alcohol hydroxyl group of 4-pyridine methanol exhibits specific activity. When exposed to acid, the hydroxyl group is easily protonated, which enhances its nucleophilicity and can participate in the esterification reaction. In the case of carboxylic acid, under suitable catalytic conditions, corresponding ester compounds can be formed.
    And the 3,5-dichloro-methyl part, the chlorine atom has an electron-absorbing induction effect, which reduces the electron cloud density of the methyl group. This structural feature causes methyl activity to change and is prone to substitution reactions. For example, under the action of nucleophiles, chlorine atoms can be replaced to form new carbon-heterobond compounds.
    In addition, the compound may participate in redox reactions because it contains a variety of active groups. Pyridine rings can be oxidized under specific conditions, and alcohol hydroxyl groups can also be oxidized to aldehyde or carboxyl groups, depending on the reaction conditions and the reagents used.
    Due to the particularity of the structure, 4-pyridyl methanol, 3,5-dichloro-methyl - may have potential application value in the field of organic synthesis and can be used as key intermediates for constructing more complex organic molecular structures.
    What are the common uses of 4-pyridinemethanol, 3,5-dichloro-methyl-
    4-Pyridyl methanol, 3,5-dichloromethyl, has a variety of common uses. In the field of organic synthesis, it is often a key raw material, and it can build complex organic structures through various reaction pathways. For example, under the catalysis of alkali with specific halogenated hydrocarbons, nucleophilic substitution reactions can be carried out to obtain pyridine derivatives modified with different substituents. Such derivatives are of great significance in pharmaceutical chemistry or have potential biological activities, and are expected to be developed into new drugs.
    In the field of materials science, polymers prepared from this as a starting material through a series of reactions may have unique electrical and optical properties and can be applied to optoelectronic materials. For example, polymerization with conjugated monomers can produce materials with excellent luminescent properties, which can help the development of devices such as organic Light Emitting Diodes.
    In addition, it also plays an important role in the preparation of fine chemical products. Or as an intermediate, it participates in the synthesis of fine chemicals such as fragrances and pigments, giving products unique aroma or color characteristics. Its applications in different fields depend on the unique reactivity and chemical properties of the pyridine ring with methanol groups and dichloromethyl groups in its own structure, providing broad space and diverse possibilities for the development of many fields.
    What is the synthesis method of 4-pyridinemethanol, 3,5-dichloro-methyl-?
    To prepare 4-pyridyl methanol, 3,5-dichloro-methyl, you can follow the following ancient method.
    Take the pyridine first and place it in a clean reactor. At low temperature, an appropriate amount of chloromethane is added, and a catalytic agent is added to replace the chlorine atoms at the 3rd and 5th positions of the pyridine, and then 3,5-dichloropyridine is obtained. This step requires careful observation of the reaction temperature, so as not to cause side reactions if it is too high.
    Transfer 3,5-dichloropyridine to another reactor for the first time, add formaldehyde and an appropriate amount of base to promote the formylation reaction to obtain 3,5-dichloro-pyridyl formaldehyde. This process requires controlling the rate of the reaction, stirring slowly, so that each substance is mixed evenly.
    Then, by hydrogenation, the aldehyde group of 3,5-dichloro-pyridinal formaldehyde is synthesized into a hydroxyl group by using a suitable hydrogenation reagent, such as sodium borohydride or lithium aluminum hydride, to obtain 4-pyridinal methanol and 3,5-dichloro-methyl. When hydrogenating, it should be in an inert gas atmosphere to avoid excessive contact with air and prevent the reagent from failing.
    After each step of the reaction, the product needs to be refined by distillation, extraction, recrystallization, etc., to remove its impurities to achieve high purity.
    What are the applications of 4-pyridinemethanol, 3,5-dichloro-methyl?
    4-Pyridyl methanol, 3,5-dichloro-methyl - This substance is used in many fields.
    In the field of medicine, it can be a key pharmaceutical intermediate. In ancient times, medicine is related to human life and is an important technique for saving the world. This compound can be converted into a drug for treating specific diseases through a delicate synthesis path. Or it can target a certain type of inflammation and use its special chemical structure to play a role in human pharmacological reactions, just like ancient pharmacists preparing fairy herbs and medicinal pills to achieve the purpose of treating diseases.
    In the field of materials science, it also has its uses. If ancient craftsmen create exquisite utensils, this compound can be used as a raw material to participate in material synthesis. Or it can be used to prepare polymer materials with special properties, giving materials such as good stability and unique optical properties, just as ancient craftsmen gave utensils unique texture and luster.
    Furthermore, in the field of organic synthetic chemistry, it is an important cornerstone. Chemists are like ancient alchemists, using various reactions to start with 4-pyridyl methanol, 3,5-dichloro-methyl - to build complex and diverse organic molecular structures. Through ingenious reaction design, many organic compounds with different functions have been derived, expanding the boundaries of chemical research, just like the ancients explored the mystery of material changes in the process of alchemy, constantly exploring new understandings.
    What is the market outlook for 4-pyridinemethanol, 3,5-dichloro-methyl-?
    Guanfu 4-pyridyl-methanol, 3,5-dichloro-methyl, has a considerable market prospect today.
    Covers are widely used in the field of chemical synthesis. It is an important raw material in the creation of medicine. The research and development of many new drugs relies on it as a basis to become a special agent to treat various diseases in the world, so the demand for it in the pharmaceutical industry is increasing day by day.
    And in the genus of materials science, it has also emerged. With it as a quality, materials with specific properties can be made, or with excellent stability or good conductivity, suitable for electronics, optics and other fields, so it has attracted the attention of the materials science community, and the market potential is gradually emerging.
    Furthermore, in the process of pesticide preparation, 4-pyridyl methanol, 3,5-dichloro-methyl are also indispensable. After delicate synthesis, it can produce powerful and low-toxic pesticides. The prosperity of farmers' mulberry and the safety of harvesting are also popular in the agricultural field.
    However, although the market has prospects, there are also challenges. The complexity of the preparation process results in high production costs; and the stricter environmental regulations, the production process needs to meet strict standards, which are all concerns of the industry. However, over time, if we can break through the difficulties of craftsmanship and comply with environmental protection regulations, it will shine brightly in the market, add glory to various industries, and lead the progress of chemical-related industries. The prospects are limitless.