Cas no 1130309-50-0 (2-(2-Aminopyridin-4-yl)acetonitrile)

2-(2-Aminopyridin-4-yl)acetonitrile is a versatile heterocyclic building block used in organic synthesis and pharmaceutical research. Its structure features both an aminopyridine moiety and a reactive nitrile group, enabling its use in the preparation of complex heterocycles, ligands, and bioactive compounds. The compound's dual functionality allows for selective modifications, making it valuable in medicinal chemistry for the development of kinase inhibitors and other therapeutic agents. Its high purity and stability under standard conditions ensure reliable performance in coupling reactions, cyclizations, and other transformations. This intermediate is particularly useful in constructing pyridine-based scaffolds with tailored properties for drug discovery and material science applications.
2-(2-Aminopyridin-4-yl)acetonitrile structure
1130309-50-0 structure
Product Name:2-(2-Aminopyridin-4-yl)acetonitrile
CAS No:1130309-50-0
MF:C7H7N3
MW:133.150580644608
CID:1201007
PubChem ID:45382143
Update Time:2025-05-20

2-(2-Aminopyridin-4-yl)acetonitrile Chemical and Physical Properties

Names and Identifiers

    • (2-amino-4-pyridinyl)acetonitrile
    • 4-Pyridineacetonitrile, 2-amino-
    • EN300-109923
    • 1130309-50-0
    • AT18208
    • 2-(2-aminopyridin-4-yl)acetonitrile
    • AKOS006324287
    • Z1198329815
    • SCHEMBL7375163
    • 2-(2-Aminopyridin-4-yl)acetonitrile
    • Inchi: 1S/C7H7N3/c8-3-1-6-2-4-10-7(9)5-6/h2,4-5H,1H2,(H2,9,10)
    • InChI Key: WSFXXEKYYWBKOM-UHFFFAOYSA-N
    • SMILES: N1C=CC(CC#N)=CC=1N

Computed Properties

  • Exact Mass: 133.063997236g/mol
  • Monoisotopic Mass: 133.063997236g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 146
  • 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: -0.1
  • Topological Polar Surface Area: 62.7?2

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Additional information on 2-(2-Aminopyridin-4-yl)acetonitrile

2-(2-Aminopyridin-4-yl)acetonitrile: A Comprehensive Overview

2-(2-Aminopyridin-4-yl)acetonitrile (CAS No. 1130309-50-0) is a compound of significant interest in the fields of organic chemistry and materials science. This molecule, characterized by its unique structure, has garnered attention due to its potential applications in drug discovery, catalysis, and advanced materials. The compound consists of a pyridine ring substituted with an amino group at the 2-position and an acetonitrile group at the 4-position, making it a versatile building block for further chemical modifications.

Recent studies have highlighted the importance of 2-(2-Aminopyridin-4-yl)acetonitrile in the development of novel therapeutic agents. Researchers have explored its ability to act as a precursor for bioactive compounds, particularly in the design of kinase inhibitors and other enzyme-targeting molecules. The amino group on the pyridine ring provides a site for further functionalization, enabling the creation of diverse derivatives with enhanced biological activity.

The synthesis of CAS No. 1130309-50-0 has been optimized through various methodologies, including microwave-assisted synthesis and catalytic cross-coupling reactions. These advancements have not only improved the yield but also reduced the environmental footprint of its production. The compound's stability under various reaction conditions makes it an ideal candidate for large-scale manufacturing in the pharmaceutical and chemical industries.

In terms of applications, 2-(2-Aminopyridin-4-yl)acetonitrile has shown promise in the field of materials science. Its ability to form coordination complexes with transition metals has led to its use in the development of new catalysts for organic transformations. Additionally, researchers have investigated its potential as a component in advanced materials such as conductive polymers and metal-organic frameworks (MOFs), where its electronic properties play a crucial role.

The latest research on CAS No. 1130309-50-0 has focused on its role in drug delivery systems. By modifying the acetonitrile group, scientists have developed prodrugs that exhibit improved solubility and bioavailability. These findings underscore the compound's versatility and its potential to address unmet needs in pharmaceutical development.

From a structural perspective, 2-(2-Aminopyridin-4-yl)acetonitrile exhibits a planar geometry due to the aromaticity of the pyridine ring. This planarity contributes to its electronic properties, making it suitable for applications in optoelectronics and sensor technologies. Recent computational studies have provided deeper insights into its electronic structure, paving the way for its use in next-generation electronic devices.

In conclusion, CAS No. 1130309-50-0, or 2-(2-Aminopyridin-4-yl)acetonitrile, is a multifaceted compound with a wide range of applications across various scientific disciplines. Its unique structure, coupled with recent advancements in synthesis and application development, positions it as a key player in future innovations within chemistry and materials science.

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