echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Production Process of 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE

    The Production Process of 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE

    • Last Update: 2023-05-09
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Introduction:


    4-Chloro-5-methoxypyridaazin-3(2H)-one, also known as 3,5-dimethyl-4-nitro-2H-pyrazolo[3,4-d]pyrimidine, is a synthetic organic compound that is widely used in various applications, including as an intermediate in the production of pharmaceuticals, agrochemicals, and other chemical products.
    The production process of 4-chloro-5-methoxypyridaazin-3(2H)-one involves several stages, including synthesis, purification, and isolation of the final product.


    Synthesis:


    The synthesis of 4-chloro-5-methoxypyridaazin-3(2H)-one typically involves several steps, including the reaction of a nitrogen compound with a carbonyl compound to form an imine, followed by a series of condensation and substitution reactions to produce the final product.
    The specific synthesis route used can vary depending on the manufacturer and the desired product specifications.


    Purification:


    After the synthesis of 4-chloro-5-methoxypyridaazin-3(2H)-one, the product is typically purified to remove any impurities that may have been introduced during the synthesis process.
    This can involve a variety of techniques, including crystallization, distillation, and chromatography.


    Isolation:


    After purification, the 4-chloro-5-methoxypyridaazin-3(2H)-one is typically isolated from any remaining impurities and other byproducts.
    This can involve additional purification steps, such as recrystallization or distillation, as well as the formation of cakes or other solid forms.


    Physical and Chemical Properties:


    4-chloro-5-methoxypyridaazin-3(2H)-one is a yellow or off-white solid with a melting point of between 140-145°C.
    The compound is highly soluble in water and various organic solvents, such as ethanol and methanol.


    Applications:


    4-chloro-5-methoxypyridaazin-3(2H)-one is used in a variety of applications, including as an intermediate in the production of pharmaceuticals, such as anti-inflammatory and anti-bacterial drugs, and agrochemicals, such as herbicides and pesticides.
    The compound is also used in research and development, as a building block for the synthesis of other organic compounds.


    Conclusion:


    The production process of 4-chloro-5-methoxypyridaazin-3(2H)-one involves several stages, including synthesis, purification, and isolation of the final product.
    The compound is widely used in various applications, including pharmaceuticals, agrochemicals, and research and development.
    The specific production process and applications of 4-chloro-5-methoxypyridaazin-3(2H)-one can vary depending on the manufacturer and the desired product specifications.


    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.