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1,3,5-trimethylbarbituric acid

  • Name: 1,3,5-trimethylbarbituric acid
  • CAS: 7358-61-4
  • Purity: 99%
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  • Description

    Quality products?make an important contribution to long-term revenue and profitability. Chinese Manufacturer supply 1,3,5-trimethylbarbituric acid 7358-61-4 in stock with high standard

    1.What is the 1,3,5-trimethylbarbituric acid ?

    1,3,5-trimethylbarbituric acid is a white crystalline solid with the molecular formula C9H12N2O3. It is a derivative of barbituric acid, known for its sedative and hypnotic effects, and is soluble in water. 1,3,5-trimethylbarbituric acid is commonly used as a reagent in organic chemistry reactions and plays a significant role in the synthesis of pharmaceuticals and other organic compounds.

    2.What is the CAS number for 1,3,5-trimethylbarbituric acid ?

    The CAS number of 1,3,5-trimethylbarbituric acid is 7358-61-4.

    3.What are another words for 1,3,5-trimethylbarbituric acid ?

    Synonyms?for?1,3,5-trimethylbarbituric acid 7358-61-4:Barbituricacid, 1,3,5-trimethyl- (6CI,7CI,8CI); 1,3,5-Trimethylbarbituric acid; NSC120716

    4.What is 1,3,5-trimethylbarbituric acid (7358-61-4) used for?

    Used in Pharmaceutical Industry:
    1,3,5-trimethylbarbituric acid is used as an intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and potential therapeutic applications.
    Used in Medicinal Chemistry:
    1,3,5-trimethylbarbituric acid is used as a compound in medicinal chemistry research for its potential as a treatment for cancer and other diseases, highlighting its importance in drug development.
    Used in Organic Chemistry:
    1,3,5-trimethylbarbituric acid is used as a reagent in organic chemistry reactions due to its solubility in water and its ability to participate in a wide range of chemical processes.

    InChI:InChI=1/C7H10N2O3/c1-4-5(10)8(2)7(12)9(3)6(4)11/h4H,1-3H3

    Relevant articles related to 1,3,5-trimethylbarbituric acid:

    Article

    Source

    Stereoselective intramolecular coupling of barbituric acids with aliphatic ketones and O-methyl oximes by electroreduction: Radical cyclization mechanism supported by DFT study

    Kise, Naoki,Tuji, Takashi,Sakurai, Toshihiko

    , p. 1790 - 1793 (2016)

    Method for synthesizing 5-substituted barbituric acid derivative under catalysis of rare earth chloride

    -

    Paragraph 0023-0025, (2020/01/03)

    Thermophysical study of several barbituric acid derivatives by differential scanning calorimetry (DSC)

    Temprado, Manuel,Roux, Maria Victoria,Ros, Francisco,Notario, Rafael,Segura, Marta,Chickos, James S.

    experimental part, p. 263 - 268 (2011/10/05)

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