Cas no 720660-12-8 (3-Pyridinemethanamine,6-amino-4-methyl-)

6-Amino-4-methyl-3-pyridinemethanamine is a heterocyclic amine derivative with potential applications in pharmaceutical and agrochemical synthesis. Its pyridine core, substituted with an amino group at the 6-position and a methyl group at the 4-position, provides a versatile scaffold for further functionalization. The compound’s structural features make it valuable as a building block in the development of bioactive molecules, particularly in medicinal chemistry for targeting nitrogen-containing heterocycles. Its stability and reactivity under controlled conditions allow for precise modifications, enabling its use in complex synthetic pathways. The presence of both amino and methyl groups enhances its utility in nucleophilic substitution and coupling reactions, offering flexibility in drug discovery and material science applications.
3-Pyridinemethanamine,6-amino-4-methyl- structure
720660-12-8 structure
Product Name:3-Pyridinemethanamine,6-amino-4-methyl-
CAS No:720660-12-8
MF:C7H11N3
MW:137.182340860367
CID:558400
PubChem ID:9813140
Update Time:2025-05-23

3-Pyridinemethanamine,6-amino-4-methyl- Chemical and Physical Properties

Names and Identifiers

    • 3-Pyridinemethanamine,6-amino-4-methyl-
    • 3-Pyridinemethanamine,6-amino-4-methyl-(9CI)
    • 5-(aminomethyl)-4-methylpyridin-2-amine
    • 720660-12-8
    • YYCHPXKRSSCCMO-UHFFFAOYSA-N
    • SCHEMBL554353
    • Inchi: 1S/C7H11N3/c1-5-2-7(9)10-4-6(5)3-8/h2,4H,3,8H2,1H3,(H2,9,10)
    • InChI Key: YYCHPXKRSSCCMO-UHFFFAOYSA-N
    • SMILES: N1C(=CC(C)=C(C=1)CN)N

Computed Properties

  • Exact Mass: 137.095297364g/mol
  • Monoisotopic Mass: 137.095297364g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 105
  • 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: -0.3
  • Topological Polar Surface Area: 64.9?2

3-Pyridinemethanamine,6-amino-4-methyl- Pricemore >>

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3-Pyridinemethanamine,6-amino-4-methyl- Related Literature

Additional information on 3-Pyridinemethanamine,6-amino-4-methyl-

Introduction to 3-Pyridinemethanamine, 6-amino-4-methyl- (CAS No. 720660-12-8)

3-Pyridinemethanamine, 6-amino-4-methyl- (CAS No. 720660-12-8) is a versatile organic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound, also known as 6-Amino-4-methylpyridine-3-methanamine, is characterized by its unique structural features and potential biological activities. Its molecular formula is C9H12N3, and it has a molecular weight of approximately 158.21 g/mol.

The chemical structure of 3-Pyridinemethanamine, 6-amino-4-methyl- consists of a pyridine ring with a methyl group at the 4-position, an amino group at the 6-position, and an amine functional group attached to the pyridine ring at the 3-position. This combination of functional groups imparts the compound with distinct chemical properties and reactivity, making it a valuable building block in the synthesis of more complex molecules.

In recent years, 3-Pyridinemethanamine, 6-amino-4-methyl- has been extensively studied for its potential applications in drug discovery and development. One of the key areas of interest is its role as a precursor in the synthesis of novel pharmaceutical agents. The presence of multiple functional groups allows for a wide range of chemical modifications, enabling researchers to tailor the compound's properties for specific therapeutic targets.

A notable example of its application is in the development of inhibitors for various enzymes and receptors. For instance, studies have shown that derivatives of 3-Pyridinemethanamine, 6-amino-4-methyl- can exhibit potent inhibitory activity against kinases, which are important targets in cancer therapy. Kinases play crucial roles in cell signaling pathways, and their dysregulation is often associated with the development and progression of various cancers.

Beyond its use as a synthetic intermediate, 3-Pyridinemethanamine, 6-amino-4-methyl- has also been investigated for its direct biological activities. Research has demonstrated that this compound can modulate certain cellular processes, such as apoptosis and inflammation. These findings suggest that it may have therapeutic potential in treating diseases characterized by aberrant cell death or chronic inflammation.

In addition to its pharmaceutical applications, 3-Pyridinemethanamine, 6-amino-4-methyl- has found use in other areas of scientific research. For example, it has been employed as a ligand in coordination chemistry to form complexes with metal ions. These complexes can exhibit interesting electronic and magnetic properties, making them useful in materials science and catalysis.

The synthesis of 3-Pyridinemethanamine, 6-amino-4-methyl- typically involves multi-step procedures that leverage well-established organic chemistry techniques. Common synthetic routes include the reaction of appropriate pyridine derivatives with amino acids or other nitrogen-containing reagents. The choice of synthetic method depends on factors such as yield, purity, and scalability.

To ensure the quality and purity of 3-Pyridinemethanamine, 6-amino-4-methyl-, rigorous analytical methods are employed during its production and characterization. Techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and high-performance liquid chromatography (HPLC) are commonly used to verify the compound's identity and assess its purity.

In conclusion, 3-Pyridinemethanamine, 6-amino-4-methyl- (CAS No. 720660-12-8) is a multifaceted compound with significant potential in various scientific and pharmaceutical applications. Its unique chemical structure and versatile reactivity make it an invaluable tool for researchers working in medicinal chemistry, drug discovery, and related fields. As ongoing research continues to uncover new insights into its properties and applications, this compound is likely to play an increasingly important role in advancing our understanding of biological systems and developing novel therapeutic agents.

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