Cas no 81333-07-5 (4-Pyrimidinecarboxamide,6-amino-)

4-Pyrimidinecarboxamide,6-amino- is a pyrimidine derivative characterized by its amino and carboxamide functional groups, which confer reactivity and versatility in synthetic chemistry applications. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and heterocyclic compounds, owing to its ability to participate in nucleophilic substitution and condensation reactions. Its stable crystalline structure and high purity make it suitable for precise research and industrial processes. The presence of both amino and carboxamide groups enhances its utility in constructing complex molecular frameworks, particularly in medicinal chemistry for developing bioactive molecules. Proper handling and storage are recommended to maintain its integrity.
4-Pyrimidinecarboxamide,6-amino- structure
81333-07-5 structure
Product Name:4-Pyrimidinecarboxamide,6-amino-
CAS No:81333-07-5
MF:C5H6N4O
MW:138.127339839935
CID:708050
PubChem ID:840530
Update Time:2025-11-02

4-Pyrimidinecarboxamide,6-amino- Chemical and Physical Properties

Names and Identifiers

    • 4-Pyrimidinecarboxamide,6-amino-
    • 6-Amino-pyrimidin-4-carbonsaeure-amid
    • 6-amino-pyrimidine-4-carboxylic acid amide
    • 6-aminopyrimidine-4-carboxamide
    • 81333-07-5
    • AKOS006274760
    • Oprea1_496381
    • SCHEMBL3032664
    • SB56581
    • Inchi: 1S/C5H6N4O/c6-4-1-3(5(7)10)8-2-9-4/h1-2H,(H2,7,10)(H2,6,8,9)
    • InChI Key: JLTSEIZANHBJML-UHFFFAOYSA-N
    • SMILES: O=C(C1C=C(N)N=CN=1)N

Computed Properties

  • Exact Mass: 138.05400
  • Monoisotopic Mass: 138.05416083g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 138
  • 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
  • XLogP3: -0.9
  • Topological Polar Surface Area: 94.9?2

Experimental Properties

  • PSA: 94.89000
  • LogP: 0.43920

4-Pyrimidinecarboxamide,6-amino- Pricemore >>

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4-Pyrimidinecarboxamide,6-amino- Related Literature

Additional information on 4-Pyrimidinecarboxamide,6-amino-

Comprehensive Guide to 4-Pyrimidinecarboxamide,6-amino- (CAS No. 81333-07-5): Properties, Applications, and Market Insights

4-Pyrimidinecarboxamide,6-amino- (CAS No. 81333-07-5) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its pyrimidine backbone and carboxamide functional group, serves as a critical intermediate in the synthesis of various bioactive molecules. Researchers and industry professionals frequently search for 6-amino-4-pyrimidinecarboxamide due to its versatile applications in drug development and material science.

The molecular structure of 4-Pyrimidinecarboxamide,6-amino- includes a pyrimidine ring substituted with an amino group at the 6-position and a carboxamide group at the 4-position. This unique arrangement contributes to its reactivity and utility in heterocyclic chemistry. Recent studies highlight its role in the design of kinase inhibitors, which are pivotal in targeted cancer therapies. The growing demand for small molecule drugs has further amplified interest in this compound.

In the pharmaceutical industry, 4-Pyrimidinecarboxamide,6-amino- is often utilized as a building block for nucleoside analogs and antiviral agents. Its ability to mimic natural nucleobases makes it invaluable in the development of treatments for viral infections, including those caused by RNA viruses. Additionally, its derivatives are explored for their potential in neurodegenerative disease research, addressing a pressing global health concern.

From a commercial perspective, the market for 6-amino-4-pyrimidinecarboxamide is expanding, driven by advancements in precision medicine and biopharmaceuticals. Suppliers and manufacturers are increasingly focusing on scalable synthesis methods to meet the rising demand. Analytical techniques such as HPLC and NMR spectroscopy are essential for ensuring the purity and quality of this compound, which is often supplied as a white to off-white crystalline powder.

Environmental and safety considerations are also paramount when handling 4-Pyrimidinecarboxamide,6-amino-. While it is not classified as hazardous under standard regulations, proper laboratory practices should be followed to minimize exposure. Researchers frequently inquire about its solubility (e.g., in DMSO or water) and storage conditions (typically 2-8°C), reflecting the compound's sensitivity to moisture and temperature.

Innovations in green chemistry have spurred interest in eco-friendly synthesis routes for CAS 81333-07-5. Catalytic methods and solvent-free reactions are being investigated to reduce waste and improve efficiency. These developments align with the broader trend toward sustainable pharmaceutical production, a topic of high relevance in both academic and industrial circles.

For those seeking reliable sources of 4-Pyrimidinecarboxamide,6-amino-, it is advisable to consult certified suppliers who provide comprehensive analytical data sheets (COA) and material safety data sheets (MSDS). The compound's pricing and availability may vary based on purity grades (e.g., >98% by HPLC) and order volumes. Bulk procurement is common among contract research organizations (CROs) and large-scale pharmaceutical manufacturers.

In summary, 4-Pyrimidinecarboxamide,6-amino- (CAS No. 81333-07-5) is a multifaceted compound with broad applications in drug discovery, biochemistry, and material science. Its role in cutting-edge research, coupled with evolving market dynamics, ensures its continued relevance. As scientific inquiries into heterocyclic compounds and targeted therapies progress, this molecule is poised to remain a key player in innovative solutions for global health challenges.

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