echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Popular Keywords > Keyword List P > pyridine

    pyridine

    Check the news of pyridine. Find top topics, trends and opinion of pyridine you need on echemi.com.
    • The Production Process of 5-Methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

      Time of Update: 2023-05-02
      The production process of 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine is a complex chemical reaction that involves several steps and requires careful control and monitoring of temperatures, pressures, and other variables. The production process of 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine is a complex chemical reaction that involves several steps and requires careful control and monitoring of temperatures, pressures, and other variables.
    • The Instruction of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      It is important to adhere to the following safety guidelines to minimize potential risks: Proper protective equipment: Wear appropriate personal protective equipment (PPE), including impervious gloves, safety glasses or goggles, and a lab coat, when handling 2-Bromo-3-fluoroimidazo[1,2-d]pyridine.
    • The Production Process of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      This compound is synthesized by a multi-step process that involves the reaction of N-bromosuccinimide with 2,6-dibromomethylamino-4-oxocyclohex-1-ene in the presence of a Lewis acid catalyst. This compound is synthesized by a multi-step process that involves the reaction of N-bromosuccinimide with 2,6-dibromomethylamino-4-oxocyclohex-1-ene in the presence of a Lewis acid catalyst.
    • The Synthetic Routes of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      Dimethylformamide (DMF) synthesis of 6-bromo-8-fluoroimidazo[1,2-a]pyridine This route involves the condensation of 2-fluoro-6-nitro-7H-imidazo[1,2-d][1,4]benzoxazepine with 2-bromopyridine in the presence of DMF at high temperature. Dimethylformamide (DMF) synthesis of 6-bromo-8-fluoroimidazo[1,2-a]pyridine This route involves the condensation of 2-fluoro-6-nitro-7H-imidazo[1,2-d][1,4]benzoxazepine with 2-bromopyridine in the presence of DMF at high temperature.
    • The Safety of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      Section 3: Toxicity and Safety There is limited data available on the toxicity and safety of 6-Br-8-F-ImPy. However, studies on similar compounds have shown that they can be toxic to living organisms, with potential effects on the liver, kidneys, and central nervous system.
    • The Upstream and Downstream products of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      Some of the downstream products of this compound include: Anticancer drugs: 6-bromo-8-fluoroimidazo[1,2-a]pyridine is used as an intermediate in the synthesis of several anticancer drugs, such as fluorouracil and its derivatives.
    • The Applications of 6-Bromo-8-fluoroimidazo[1,2-a]pyridine

      Time of Update: 2023-04-26
      It is used as a building block for the synthesis of other compounds, an intermediate in the production of pesticides, pharmaceuticals, dyes and pigments, surfactants, leather chemicals and water treatment chemicals.
    • Issue 48/2012 - Anhui pyridine alkali engineering center settled in Guoxing Biotechnology

      Time of Update: 2022-11-12
      (Zhu Yuan) Anhui pyridine alkali engineering center settled in Guoxing BiotechnologyA few days ago, Anhui Pyridine Base Engineering Technology Research Center was included in the 2012 provincial engineering center establishment plan.
    • A new strategy for light-controlled release of pyridine compounds proposed by chemistry

      Time of Update: 2022-08-12
      . Recently, Fang Xiaohong, a researcher at the Key Laboratory of Molecular Nanostructure and Nanotechnology, Institute of Chemistry, Chinese Academy of Sciences, has developed a new strategy to release pyridine by inhibiting intramolecular electron transfer in the photolysis of N-alkylpyridinium salt in aqueous solution .
    • Nankai team: Organoboron "knocks on" the "new door" of pyridine drug synthesis

      Time of Update: 2022-04-27
      A few days ago, the research group of Wang Xiaochen from the School of Chemistry of Nankai University used organoboron as a catalyst to ingeniously activate the reactivity of the C3 position of the pyridine ring, and successfully "knocked open" a "new door" for the efficient synthesis of pyridine compounds .
    • Corteva: The global brand name of the third generation of novel pyridine amide active substances is Haviza™

      Time of Update: 2022-03-02
      In addition, the Haviza brand will assure farmers of: Any product bearing this logo has the advantage of Corteva Agriscience's outstanding research, development and testing . In addition, the Haviza brand will assure farmers of: Any product bearing this logo has the advantage of Corteva Agriscience's outstanding research, development and testing .
    • Hydroquinone, pyridine redox resin

      Time of Update: 2022-01-01
      These quinone-based vinyl compounds can also be copolymerized with divinylbenzene and the like to form a redox resin . The reaction equation is as follows:(2) PyridinesNicotinamide was added to the chloromethylated polystyrene resin to obtain the following redox resin .
    • Production method of borane-pyridine complex

      Time of Update: 2021-08-28
      Borane-pyridine complex is very harmful, so in the process of transportation, there will be special gas tanks for equipment, which can prevent explosions or other dangerous accidents . After understanding what is the production method of filtering out the borane-pyridine complex , everyone can make some understanding .
    • Small pyridine and soraphinist: good effect against liver cancer

      Time of Update: 2020-12-22
      Figure 2 Cell Suppression Experiment As shown in Figure II, the inhibition of soraphinib on liver cancer cells (PRF-PLC-5, HCC-Lm3) was significantly enhanced by the association of soramine and soraphinib, in which THE PRF-PLC-5, Sorafinib (SORA) single-use IC50 was 14.52μM, while Sorafinib and For liver cancer cell HCC-Lm3, soraphine (SORA) single-use IC50 is 21.29 m, and Soraphini and IC50 for small niacin (SORA-BBM) IC50 is 8.442 m.
    • HER2 pan-cancer species use the finger can wait for the next city of pyridine.

      Time of Update: 2020-07-29
      The new drug her1, HER2 and HER4 tyrosine kinase irreversible oral inhibitors developed in China have been approved in 2018 for the treatment of HER2-positive advanced breast cancer This year ASCO's P

    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.