Cas no 1256633-31-4 (2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile)

2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile structure
1256633-31-4 structure
Product Name:2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile
CAS No:1256633-31-4
MF:C9H9N3O2
MW:191.186661481857
MDL:MFCD18070992
CID:1024899
PubChem ID:53217450
Update Time:2025-07-22

2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile Chemical and Physical Properties

Names and Identifiers

    • 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile
    • 2-Methyl-2-(5-nitro-2-pyridinyl)propanenitrile
    • ACMC-209azz
    • AK-91953
    • ANW-18525
    • BD230125
    • CTK8A9592
    • SureCN357918
    • A890046
    • MFCD18070992
    • 1256633-31-4
    • 2-Pyridineacetonitrile, alpha,alpha-dimethyl-5-nitro-
    • SY011020
    • DB-019545
    • 2-Methyl-2-(5-nitro-pyridin-2-yl)-propionitrile
    • SCHEMBL357918
    • EN300-1866473
    • WGTZNLRJXIIZEB-UHFFFAOYSA-N
    • AC3419
    • BS-19937
    • CS-0211978
    • SB32272
    • AKOS015907973
    • DTXSID80682489
    • MDL: MFCD18070992
    • Inchi: 1S/C9H9N3O2/c1-9(2,6-10)8-4-3-7(5-11-8)12(13)14/h3-5H,1-2H3
    • InChI Key: WGTZNLRJXIIZEB-UHFFFAOYSA-N
    • SMILES: [O-][N+](C1=CN=C(C=C1)C(C#N)(C)C)=O

Computed Properties

  • Exact Mass: 191.069476538g/mol
  • Monoisotopic Mass: 191.069476538g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 274
  • 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: 82.5?2

2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile Pricemore >>

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Additional information on 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile

Recent Advances in the Study of 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile (CAS: 1256633-31-4)

The compound 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile (CAS: 1256633-31-4) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This nitropyridine derivative has shown promising potential in various applications, particularly in drug discovery and development. Recent studies have focused on its synthesis, physicochemical properties, and biological activities, shedding light on its mechanism of action and therapeutic possibilities.

One of the key breakthroughs in the study of this compound is its role as a versatile intermediate in the synthesis of more complex pharmaceutical agents. Researchers have developed novel synthetic routes to produce 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile with high yield and purity, which is crucial for its application in medicinal chemistry. The compound's unique structure, featuring both a nitropyridine moiety and a nitrile group, makes it particularly interesting for further chemical modifications.

Recent pharmacological investigations have revealed that 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile exhibits interesting biological activities. Preliminary studies suggest potential inhibitory effects on certain enzymes involved in inflammatory pathways, making it a candidate for the development of anti-inflammatory drugs. Additionally, its interaction with specific protein targets has been characterized through molecular docking studies, providing insights into its binding modes and structure-activity relationships.

The stability and solubility profile of 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile have been thoroughly investigated in recent months. These studies are particularly important for understanding its pharmacokinetic properties and potential formulation challenges. Researchers have employed advanced analytical techniques, including HPLC-MS and NMR spectroscopy, to characterize the compound's behavior under various physiological conditions.

Looking forward, the current research trajectory suggests several promising directions for 2-Methyl-2-(5-nitropyridin-2-yl)propanenitrile. Ongoing studies are exploring its potential as a scaffold for developing novel kinase inhibitors and its application in targeted drug delivery systems. The compound's unique chemical properties continue to make it a valuable subject of investigation in both academic and industrial research settings.

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