Cas no 5194-33-2 (5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI))

5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI) is a pyrimidine derivative with potential applications in pharmaceutical and agrochemical research. Its structural features, including the 2-methyl substitution and carboxamide functional group, make it a valuable intermediate in the synthesis of biologically active compounds. The compound's pyrimidine core is known for its role in nucleobase chemistry, suggesting utility in the development of novel therapeutics or crop protection agents. Its defined purity and stability under standard conditions ensure consistent performance in synthetic workflows. Researchers may leverage this compound for its modular reactivity, enabling further functionalization or incorporation into larger molecular frameworks.
5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI) structure
5194-33-2 structure
Product Name:5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI)
CAS No:5194-33-2
MF:C6H7N3O
MW:137.139280557632
CID:1021734
PubChem ID:45080502
Update Time:2025-05-22

5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI) Chemical and Physical Properties

Names and Identifiers

    • 5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI)
    • 2-methylpyrimidine-5-carboxamide
    • DTXSID20664002
    • SB57666
    • AKOS006365984
    • 5194-33-2
    • SCHEMBL669121
    • MDL: MFCD00187868
    • Inchi: 1S/C6H7N3O/c1-4-8-2-5(3-9-4)6(7)10/h2-3H,1H3,(H2,7,10)
    • InChI Key: GMDRUGZBWUTQMX-UHFFFAOYSA-N
    • SMILES: O=C(C1C=NC(C)=NC=1)N

Computed Properties

  • Exact Mass: 137.059
  • Monoisotopic Mass: 137.059
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 129
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 68.9A^2
  • XLogP3: -0.5

5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI) Pricemore >>

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Additional information on 5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI)

5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI)

5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI), also known as CAS No. 5194-33-2, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound belongs to the class of pyrimidine derivatives, which have been extensively studied due to their diverse biological activities and potential therapeutic applications. The structure of 5-Pyrimidinecarboxamide, 2-methyl- consists of a pyrimidine ring with a methyl group at position 2 and a carboxamide group at position 5. This unique arrangement contributes to its distinct chemical properties and biological functions.

Recent studies have highlighted the importance of pyrimidine derivatives in drug discovery, particularly in the development of anticancer agents. The 5-Pyrimidinecarboxamide, 2-methyl- structure has been shown to exhibit promising antiproliferative activity against various cancer cell lines. Researchers have utilized advanced computational methods, such as molecular docking and QSAR modeling, to understand the binding interactions of this compound with key oncogenic targets. These findings underscore its potential as a lead compound for further optimization in cancer therapy.

In addition to its anticancer properties, 5-Pyrimidinecarboxamide, 2-methyl- has also been investigated for its role in modulating cellular signaling pathways. For instance, studies have demonstrated its ability to inhibit specific kinases involved in cell proliferation and survival. This makes it a valuable tool in understanding the molecular mechanisms underlying various diseases, including neurodegenerative disorders and inflammatory conditions.

The synthesis of 5-Pyrimidinecarboxamide, 2-methyl- involves a multi-step process that typically begins with the preparation of the pyrimidine ring followed by functionalization at specific positions. Recent advancements in synthetic chemistry have enabled more efficient and scalable methods for producing this compound. For example, the use of microwave-assisted synthesis has significantly reduced reaction times while maintaining high yields.

From an analytical standpoint, CAS No. 5194-33-2 has been characterized using various spectroscopic techniques such as NMR and IR spectroscopy. These analyses provide critical insights into the compound's molecular structure and purity. Furthermore, mass spectrometry has been employed to confirm its molecular formula and detect any impurities that may arise during synthesis.

Looking ahead, the continued exploration of 5-Pyrimidinecarboxamide, 2-methyl- is expected to yield further insights into its therapeutic potential. Collaborative efforts between academic institutions and pharmaceutical companies are paving the way for preclinical studies aimed at evaluating its safety and efficacy in vivo. Such research is crucial for translating laboratory findings into clinical applications that can benefit patients worldwide.

In conclusion, 5-Pyrimidinecarboxamide, 2-methyl- (7CI,8CI) or CAS No. 5194-33-2 stands as a testament to the ongoing advancements in chemical research. Its unique structure, coupled with emerging scientific discoveries, positions it as a promising candidate in the development of innovative therapeutic agents.

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