Cas no 71858-92-9 (3-(4-methylpyridin-2-yl)propanenitrile)

3-(4-Methylpyridin-2-yl)propanenitrile is a versatile nitrile derivative featuring a pyridine moiety with a methyl substituent at the 4-position. This compound serves as a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive nitrile group enables further functionalization, while the pyridine ring enhances its utility in coordination chemistry and catalysis. The methyl group at the 4-position can influence electronic and steric properties, making it useful in fine-tuning reactivity for targeted applications. The compound is typically handled under standard laboratory conditions, with attention to stability and compatibility. Its well-defined structure ensures reproducibility in synthetic workflows.
3-(4-methylpyridin-2-yl)propanenitrile structure
71858-92-9 structure
Product Name:3-(4-methylpyridin-2-yl)propanenitrile
CAS No:71858-92-9
MF:C9H10N2
MW:146.189101696014
CID:1116535
PubChem ID:12508833
Update Time:2025-06-29

3-(4-methylpyridin-2-yl)propanenitrile Chemical and Physical Properties

Names and Identifiers

    • 4-methyl-2-Pyridinepropanenitrile
    • 3-(4-methylpyridin-2-yl)propanenitrile
    • DTXSID701300062
    • EN300-1843850
    • 71858-92-9
    • Inchi: 1S/C9H10N2/c1-8-4-6-11-9(7-8)3-2-5-10/h4,6-7H,2-3H2,1H3
    • InChI Key: DSPRXCBKGXZTBV-UHFFFAOYSA-N
    • SMILES: N1C=CC(C)=CC=1CCC#N

Computed Properties

  • Exact Mass: 146.084398327g/mol
  • Monoisotopic Mass: 146.084398327g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 156
  • 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: 1.2
  • Topological Polar Surface Area: 36.7?2

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Additional information on 3-(4-methylpyridin-2-yl)propanenitrile

3-(4-Methylpyridin-2-yl)Propanenitrile: A Comprehensive Overview

3-(4-Methylpyridin-2-yl)Propanenitrile, also known by its CAS registry number CAS No. 71858-92-9, is a versatile organic compound that has garnered significant attention in various fields of chemistry and chemical engineering. This compound, with the molecular formula C10H11N, belongs to the class of nitriles and pyridine derivatives, making it a valuable intermediate in the synthesis of diverse chemical products.

The structure of 3-(4-Methylpyridin-2-yl)Propanenitrile consists of a pyridine ring substituted with a methyl group at the 4-position and a propanenitrile group at the 2-position. This unique arrangement imparts the compound with distinct chemical properties, including its reactivity in various synthetic reactions. The nitrile group is particularly reactive, making it a prime candidate for further functionalization in organic synthesis.

In recent years, advancements in synthetic methodologies have significantly enhanced our ability to produce 3-(4-Methylpyridin-2-yl)Propanenitrile on an industrial scale. Researchers have explored various routes to optimize the synthesis process, focusing on improving yield, reducing reaction time, and minimizing environmental impact. For instance, studies have demonstrated that catalytic hydrogenation and selective oxidation techniques can be effectively employed to synthesize this compound from readily available starting materials.

The application of 3-(4-Methylpyridin-2-yl)Propanenitrile spans across multiple industries. In the pharmaceutical sector, it serves as an intermediate in the synthesis of bioactive compounds with potential therapeutic applications. Recent studies have highlighted its role in the development of anti-inflammatory and anticancer agents, underscoring its importance in drug discovery research.

In addition to its pharmaceutical applications, 3-(4-Methylpyridin-2-yl)Propanenitrile finds utility in agrochemicals and specialty chemicals. Its ability to act as a precursor for more complex molecules makes it indispensable in the design of novel pesticides and herbicides. Moreover, ongoing research into its catalytic properties suggests potential applications in homogeneous catalysis and green chemistry.

The latest research on CAS No. 71858-92-9 has focused on understanding its electronic properties and reactivity under different conditions. Computational studies have provided insights into its molecular interactions, which are crucial for predicting its behavior in various chemical transformations. These findings have paved the way for innovative approaches to utilizing this compound in advanced materials science.

In conclusion, 3-(4-Methylpyridin-2-yl)Propanenitrile, identified by its CAS number CAS No. 71858-92-9, stands as a testament to the ingenuity of modern chemistry. Its diverse applications and ongoing research promise to unlock new possibilities across multiple disciplines, cementing its role as a key player in contemporary chemical innovation.

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