2 Pyridinemethanol 6 Chloro
pyridine pyrrole pyrazine piperidine piperazine

2-Pyridinemethanol, 6-chloro-

    Specifications

    HS Code

    979486

    Chemical Formula C6H6ClNO
    Molecular Weight 143.57
    Appearance Solid (likely white or off - white)
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Data needed
    Solubility In Organic Solvents Data needed
    Density Data needed
    Pka Value Data needed
    Vapor Pressure Data needed
    Flash Point Data needed

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    General Information
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    Frequently Asked Questions

    As a leading 2-Pyridinemethanol, 6-chloro- 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 2-Pyridinemethanol, 6-chloro-?
    2-Pyridyl methanol, 6-chlorine - The chemical properties of this substance are as follows:
    It has certain physical and chemical properties. From the perspective of physical properties, usually at room temperature and pressure, its appearance may be a specific form, either a solid or a liquid, but the specific form depends on experimental observation and accurate determination. Its melting point is also an important physical constant. The melting point characterizes the temperature at which a substance changes from a solid state to a liquid state, and the boiling point is related to the temperature at which a substance changes from a liquid state to a gas state. These values are of great significance for the identification and separation of the substance.
    In terms of chemical properties, the molecule contains chlorine atoms, pyridine rings and methanol groups, which give it unique reactivity. Chlorine atoms can participate in the substitution reaction and can be replaced by other nucleophiles. This reaction may occur under specific solvents and conditions. For example, in an alkaline environment and at an appropriate temperature, the nucleophiles attack the carbon atoms attached to the chlorine atoms, and the chlorine atoms leave to form new compounds. Pyridine rings are electron-rich aromatic heterocycles, which are aromatic and can undergo electrophilic substitution reactions. Due to the presence of nitrogen atoms, the electron cloud density distribution on the ring is uneven, and the reaction check point is selective. Methanol groups can participate in common reactions of alcohols, such as esterification reactions. Under acid catalysis, they react with carboxylic acids to form ester compounds. In this process, the hydroxyl groups and carboxylic groups are dehydrated and condensed.
    In addition, the chemical stability of the compound is also an important consideration. Under different environmental conditions, such as light, humidity, and temperature changes, its structure and properties may change. In the air, it may gradually deteriorate due to oxidation and other effects, so it is necessary to pay attention to the influence of environmental factors when storing.
    In summary, the chemical properties of 2-pyridylmethanol and 6-chlorine are rich and diverse, and many reactions and characteristics lay the foundation for their application in organic synthesis, pharmaceutical chemistry, etc. However, more experiments and studies are needed to further explore their properties.
    What are the physical properties of 2-Pyridinemethanol, 6-chloro-
    2-Pyridyl methanol, 6-chlorine, is one of the organic compounds. Its physical properties are quite important, and it is related to many properties and uses of this substance.
    In terms of its appearance, it is usually white to white crystalline powder, with a fine texture, like the cleanliness of the first snow in winter. This form is easy to observe and operate, and provides convenience for relevant personnel in many experimental and industrial processes.
    Melting point is also a key physical property. The melting point of this substance is within a certain range, and this value reflects the strength of the intermolecular force. When the outside temperature reaches the melting point, the molecule can break free from the original lattice and gradually change from the solid state to the liquid state, just like ice and snow melting, and start the journey of material morphology transformation.
    Solubility cannot be ignored. In common organic solvents, such as ethanol and acetone, this compound exhibits good solubility, just like fish entering water and fusing freely. This property provides a broad application space for it in various chemical reactions and preparation processes. It can be used as a reactant or intermediate. With good dispersion in solvents, the reaction is carried out efficiently.
    In addition, its density is relatively stable, just like a cornerstone laying the foundation for the physical state of the substance under specific conditions. The value of density allows people to accurately control its proportion and distribution in the mixture, which is crucial for preparation and quality control.
    Furthermore, the stability of the compound is also an important part of the physical properties. Under normal conditions, it can maintain a relatively stable structure, and in case of specific temperature, light or other chemical substances, the structure may change. This stability feature requires appropriate conditions during storage and transportation to ensure its quality as before.
    What is the main use of 2-Pyridinemethanol, 6-chloro-?
    2-Pyridyl methanol, 6-chlorine - This substance has a wide range of uses. In the field of medicine, it is often a key intermediate for the synthesis of many drugs. Due to the unique chemical activity of pyridine ring and chlorine atoms, it can build complex drug molecular structures through a variety of chemical reactions, which is of great significance for the development of antibacterial, anti-inflammatory, anti-tumor and other drugs. For example, in the development of some new antibacterial drugs, using this as the starting material, through multi-step reactions, specific functional groups can be introduced to enhance the binding force between drugs and bacterial targets and improve the antibacterial effect.
    In the field of materials science, it can participate in the preparation of functional materials. For example, polymerization with specific organic compounds to generate polymer materials with special optical and electrical properties, or used to make photoelectric sensors, organic Light Emitting Diodes and other devices, endowing materials with unique physical and chemical properties to meet the needs of different application scenarios.
    In the field of organic synthesis, as an important organic reagent, it provides an effective path for the synthesis of complex organic compounds. With its structural characteristics, it can participate in various reactions such as nucleophilic substitution and redox, enabling organic chemists to construct various carbon-carbon and carbon-heteroatom bonds, expanding the variety and structural diversity of organic compounds, and contributing to the development of organic synthetic chemistry.
    What is the synthesis method of 2-Pyridinemethanol, 6-chloro-?
    2-Pyridine-methanol, 6-chloro-methanol, the synthesis method is as follows:
    Take pyridine as the base first, and introduce chlorine atoms at the 6 position through halogenation. Suitable halogenating agents, such as chlorinating agents, can be selected under appropriate reaction conditions to make pyridine substitution reaction to obtain 6-chloropyridine. In this step, attention should be paid to the control of reaction temperature, time and reagent dosage to prevent side reactions.
    6-chloropyridine is methylated for several times. 6-chloropyridine is often assisted by a suitable catalyst to make 6-chloropyridine meet methanol. The choice of catalyst is very important, depending on the reaction rate and yield. In the reaction system, the reactants are mixed according to a specific stoichiometric ratio, and under a certain temperature and pressure, through catalytic action, the chlorine atoms are replaced by methanol groups, and 2-pyridyl methanol and 6-chlorine are gradually produced.
    After the reaction is completed, the product may contain impurities, which must be purified by separation and purification. Distillation, extraction, recrystallization, etc. can be used to remove impurities and obtain pure 2-pyridyl methanol and 6-chlorine products according to the physical properties of the product and impurities. < Br >
    Thus, according to the steps of halogenation, methanol and separation and purification, the compounds of 2-pyridyl methanol and 6-chlorine can be obtained.
    2-Pyridinemethanol, 6-chloro - what to pay attention to when storing and shipping
    2-Pyridyl methanol, 6-chlorine - Many things should be paid attention to when storing and transporting this substance.
    First, storage, because of its special nature, must choose a cool, dry and well-ventilated place. Avoid direct sunlight, because light may cause chemical reactions to occur, which will damage its quality. Furthermore, keep away from fires and heat sources, which may be flammable, and may be dangerous in case of open flames and hot topics. At the same time, it should be stored separately from oxidants, acids, etc., and cannot be mixed to prevent adverse consequences from interaction.
    As for transportation, make sure that the container is well sealed to prevent leakage. During transportation, the traffic should be stable to avoid bumps and collisions to prevent material leakage due to damage to the container. Transportation vehicles should also be equipped with corresponding types and quantities of fire fighting equipment and leakage emergency treatment equipment. Escort personnel must be familiar with the nature of the transported goods and emergency disposal methods, pay close attention on the way, and if there is any abnormality, deal with it immediately. In this way, the safety of 2-pyridine methanol and 6-chlorine is guaranteed during storage and transportation.