Cas no 28523-93-5 (4,5-dichloro-2-nitrobenzonitrile)

4,5-Dichloro-2-nitrobenzonitrile is a halogenated aromatic nitrile compound with a nitro substituent, commonly utilized as an intermediate in organic synthesis and pharmaceutical manufacturing. Its molecular structure, featuring both chloro and nitro functional groups, enhances reactivity in nucleophilic substitution and coupling reactions, making it valuable for constructing complex heterocyclic frameworks. The compound's high purity and stability under standard conditions ensure consistent performance in synthetic applications. It is particularly useful in agrochemical and pharmaceutical research, where precise functionalization of aromatic systems is required. Proper handling is advised due to potential irritant properties. Storage should be in a cool, dry environment, protected from light.
4,5-dichloro-2-nitrobenzonitrile structure
28523-93-5 structure
Product Name:4,5-dichloro-2-nitrobenzonitrile
CAS No:28523-93-5
MF:C7H2Cl2N2O2
MW:217.008979320526
CID:1006724
PubChem ID:13499262
Update Time:2025-11-01

4,5-dichloro-2-nitrobenzonitrile Chemical and Physical Properties

Names and Identifiers

    • 4,5-dichloro-2-nitrobenzonitrile
    • Benzonitrile, 4,5-dichloro-2-nitro-
    • FD10739
    • 3,4-DICHLORO-6-NITROBENZONITRILE
    • 28523-93-5
    • DB-330883
    • SCHEMBL11329936
    • MDL： MFCD09999944
    • Inchi： 1S/C7H2Cl2N2O2/c8-5-1-4(3-10)7(11(12)13)2-6(5)9/h1-2H
    • InChI Key： DQEOUPUFGJBXFK-UHFFFAOYSA-N
    • SMILES： ClC1C(=CC(C#N)=C(C=1)[N+](=O)[O-])Cl

Computed Properties

  • Exact Mass: 215.9493327g/mol
  • Monoisotopic Mass: 215.9493327g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 257
  • 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: 2.6
  • Topological Polar Surface Area: 69.6?2

4,5-dichloro-2-nitrobenzonitrile Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1732415-1g
4,5-Dichloro-2-nitrobenzonitrile
 28523-93-5 98%
1g
 ￥5359.00 2024-05-20

4,5-dichloro-2-nitrobenzonitrile Related Literature

Additional information on 4,5-dichloro-2-nitrobenzonitrile

Comprehensive Guide to 4,5-Dichloro-2-nitrobenzonitrile (CAS No. 28523-93-5): Properties, Applications, and Industry Insights

4,5-Dichloro-2-nitrobenzonitrile (CAS No. 28523-93-5) is a specialized organic compound widely recognized for its versatile applications in agrochemicals, pharmaceuticals, and material science. With the rising demand for nitroaromatic compounds and halogenated benzonitriles, this chemical has garnered significant attention in research and industrial sectors. Its molecular structure, featuring dichloro and nitro functional groups, contributes to unique reactivity, making it a valuable intermediate in synthetic chemistry.

In recent years, the compound has been linked to advancements in crop protection agents and pharmaceutical intermediates, aligning with global trends toward sustainable agriculture and precision medicine. Researchers frequently search for "4,5-Dichloro-2-nitrobenzonitrile synthesis" or "CAS 28523-93-5 applications," reflecting its growing relevance. The compound’s stability under controlled conditions and compatibility with cross-coupling reactions further enhance its utility in modern organic synthesis.

From an industrial perspective, 4,5-Dichloro-2-nitrobenzonitrile serves as a precursor for herbicides and fungicides, addressing the need for eco-friendly pest control solutions. Its role in developing heterocyclic compounds also positions it as a key player in drug discovery, particularly for targeting resistant pathogens. Environmental and safety studies emphasize proper handling protocols, though it is not classified under restricted categories.

Emerging technologies, such as AI-driven molecular design, have accelerated research into optimizing the compound’s derivatives. Queries like "nitrobenzonitrile derivatives in drug development" highlight its interdisciplinary appeal. Additionally, its thermal stability and solubility profile make it suitable for high-performance material applications, including polymers and coatings.

In summary, 4,5-Dichloro-2-nitrobenzonitrile (CAS No. 28523-93-5) exemplifies the intersection of innovation and practicality. As industries prioritize green chemistry and efficient synthesis routes, this compound continues to inspire cutting-edge solutions across multiple scientific domains.

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