Cas no 74502-96-8 (4-Pyrimidinecarboxamide,2,6-dimethyl-)

4-Pyrimidinecarboxamide, 2,6-dimethyl-, is a pyrimidine derivative characterized by its dimethyl substitution at the 2 and 6 positions and a carboxamide functional group at the 4-position. This structure imparts unique reactivity and potential utility in pharmaceutical and agrochemical applications, particularly as an intermediate in the synthesis of more complex heterocyclic compounds. Its well-defined molecular framework offers advantages in precision chemical synthesis, enabling controlled modifications for targeted biological activity. The compound's stability and solubility profile further enhance its suitability for research and development purposes, particularly in medicinal chemistry where pyrimidine scaffolds are valued for their bioisosteric properties.
4-Pyrimidinecarboxamide,2,6-dimethyl- structure
74502-96-8 structure
Product Name:4-Pyrimidinecarboxamide,2,6-dimethyl-
CAS No:74502-96-8
MF:C7H9N3O
MW:151.165860891342
CID:556709
Update Time:2025-06-07

4-Pyrimidinecarboxamide,2,6-dimethyl- Chemical and Physical Properties

Names and Identifiers

    • 4-Pyrimidinecarboxamide,2,6-dimethyl-
    • 4-Pyrimidinecarboxamide,2,6-dimethyl-(6CI,7CI,9CI)
    • 2,6-dimethylpyrimidine-4-carboxamide
    • Inchi: 1S/C7H9N3O/c1-4-3-6(7(8)11)10-5(2)9-4/h3H,1-2H3,(H2,8,11)
    • InChI Key: GIDQOWFSUAZVNW-UHFFFAOYSA-N
    • SMILES: C1(C)=NC(C)=CC(C(N)=O)=N1

Computed Properties

  • Exact Mass: 151.07467

Experimental Properties

  • PSA: 68.87

4-Pyrimidinecarboxamide,2,6-dimethyl- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1973791-1g
2,6-Dimethylpyrimidine-4-carboxamide
74502-96-8 98%
1g
¥5373.00 2024-07-28

Additional information on 4-Pyrimidinecarboxamide,2,6-dimethyl-

Comprehensive Overview of 4-Pyrimidinecarboxamide,2,6-dimethyl- (CAS No. 74502-96-8)

4-Pyrimidinecarboxamide,2,6-dimethyl- (CAS No. 74502-96-8) is a specialized organic compound belonging to the pyrimidine family, a class of heterocyclic aromatic compounds with significant applications in pharmaceuticals, agrochemicals, and material science. The compound features a pyrimidine core substituted with a carboxamide group and two methyl groups at the 2 and 6 positions, which contribute to its unique chemical and physical properties. Researchers and industries are increasingly interested in this compound due to its potential as a building block for drug discovery and its role in advanced material synthesis.

The growing demand for pyrimidine derivatives in medicinal chemistry has placed 4-Pyrimidinecarboxamide,2,6-dimethyl- under the spotlight. Pyrimidines are essential scaffolds in nucleobases, making them critical for DNA and RNA synthesis. This compound, in particular, is explored for its bioactivity and potential as an intermediate in the development of antiviral, anticancer, and anti-inflammatory agents. Its structural versatility allows for modifications that can enhance binding affinity and selectivity toward biological targets, a topic frequently searched by researchers in drug design forums.

In the context of green chemistry and sustainable synthesis, CAS No. 74502-96-8 has garnered attention for its potential to be synthesized using eco-friendly methodologies. Recent trends in chemical research emphasize reducing hazardous byproducts and optimizing reaction conditions. Users often search for "sustainable synthesis of pyrimidine derivatives" or "green chemistry approaches for heterocyclic compounds," highlighting the relevance of this compound in contemporary scientific discussions.

Another area of interest is the compound's application in material science. Pyrimidine-based molecules are investigated for their optical and electronic properties, making them candidates for organic semiconductors, light-emitting diodes (OLEDs), and photovoltaic devices. The methyl and carboxamide functional groups in 4-Pyrimidinecarboxamide,2,6-dimethyl- can influence its conjugation and charge transport characteristics, a subject frequently queried in academic and industrial research databases.

From an analytical perspective, the characterization of 74502-96-8 involves advanced techniques such as nuclear magnetic resonance (NMR), high-performance liquid chromatography (HPLC), and mass spectrometry (MS). These methods ensure purity and structural integrity, which are critical for its application in high-value industries. Search queries like "analytical methods for pyrimidine carboxamides" reflect the need for reliable quality control protocols.

In summary, 4-Pyrimidinecarboxamide,2,6-dimethyl- (CAS No. 74502-96-8) is a multifaceted compound with broad applicability in life sciences and advanced materials. Its structural features align with current research trends, including drug discovery, sustainable chemistry, and functional materials. As scientific inquiries continue to evolve, this compound remains a valuable subject for innovation and development.

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