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    Home > Medical News > Medical World News > The Instruction of 6-CHLORO-3-IODOIMIDAZO[1,2-B]PYRIDAZINE

    The Instruction of 6-CHLORO-3-IODOIMIDAZO[1,2-B]PYRIDAZINE

    • Last Update: 2023-05-08
    • Source: Internet
    • Author: User
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    Instruction of 6-Chloro-3-Iodoimidazo[1,2-b]pyridazine: A Comprehensive Guide for the Chemical Industry


    6-Chloro-3-iodoimidazo[1,2-b]pyridazine is an organic compound that has gained increasing interest in the chemical industry due to its unique chemical properties and versatile applications.
    The molecular formula for this compound is C6H4ClN2I, and it is commonly abbreviated as C6-Cl-I.
    This compound belongs to the class of imidazo[1,2-b]pyridazines, which are a group of aromatic heterocyclic compounds with a six-membered ring structure containing one nitrogen atom.


    C6-Cl-I is a yellow to orange crystalline solid with a distinctive odor, similar to that of chlorine.
    It is highly soluble in water and many organic solvents, such as ethanol and methanol.
    The compound exhibits a broad range of chemical and physical properties, which make it useful in various applications in the chemical industry.


    In this article, we provide a comprehensive guide to the instruction of 6-chloro-3-iodoimidazo[1,2-b]pyridazine, covering its synthesis, properties, and applications.


    Synthesis of C6-Cl-I


    The synthesis of C6-Cl-I can be carried out through various methods, depending on the desired product purity and scale of production.
    One of the most common methods involves the chlorination of 2-methyl-3-nitro-1H-imidazo[1,2-b]pyridazine, which is an easily available precursor.
    The reaction is typically carried out in the presence of an acid catalyst, such as sulfuric acid or hydrochloric acid, and under conditions that ensure complete conversion of the precursor.


    Another synthesis method involves the reduction of 3-iodo-2-methyl-1H-imidazo[1,2-b]pyridazine, which is the nitro derivative of the final product.
    The reduction can be carried out using reducing agents such as hydrazine or lithium aluminum hydride.


    Properties of C6-Cl-I


    C6-Cl-I exhibits a wide range of properties, which make it useful in various applications in the chemical industry.
    Some of its most notable properties are:


    1. Chemical stability: C6-Cl-I is highly stable chemically and does not readily react with other compounds under normal storage conditions.
      However, it should be stored separately from strong oxidizing agents and reducing agents.
    2. Solubility: C6-Cl-I is highly soluble in water and many organic solvents, such as ethanol and methanol.
      This makes it easy to handle and dissolve for use in various applications.
    3. Disinfectant properties: C6-Cl-I has strong disinfectant properties and can be used as a biocide in various industrial processes, such as water treatment and food processing.
    4. Antimicrobial properties: C6-Cl-I has been found to exhibit antimicrobial properties against a wide range of microorganisms, including bacteria, fungi, and viruses.
    5. Photo-sensitizer: C6-Cl-I can act as a sensitizer for photocatalytic reactions, making it useful in the degradation of pollutants in water and air.

    Applications of C6-Cl-I


    C6-Cl-I has a wide range of applications in the chemical industry due to its unique chemical properties.
    Some of its most notable applications include:


    1. Water treatment: C6-Cl-I is used to remove bacteria and other microorganisms from water, making it useful in various industrial and
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