Cas no 13296-87-2 (Benzamide, 2,4-dinitro-)

Benzamide, 2,4-dinitro- is a nitro-substituted aromatic compound characterized by the presence of two nitro groups at the 2- and 4-positions of the benzene ring. This derivative of benzamide exhibits notable reactivity due to its electron-withdrawing nitro substituents, making it useful in organic synthesis and as an intermediate in the preparation of more complex chemical structures. Its high purity and well-defined molecular properties ensure consistent performance in applications such as pharmaceuticals, agrochemicals, and specialty materials. The compound's stability under controlled conditions and predictable behavior in reactions contribute to its utility in research and industrial processes. Proper handling and storage are recommended due to its potential sensitivity to heat and shock.
Benzamide, 2,4-dinitro- structure
Benzamide, 2,4-dinitro- structure
Product Name:Benzamide, 2,4-dinitro-
CAS No:13296-87-2
MF:C7H5N3O5
MW:211.131701231003
CID:1236581
PubChem ID:3733518
Update Time:2025-10-10

Benzamide, 2,4-dinitro- Chemical and Physical Properties

Names and Identifiers

    • Benzamide, 2,4-dinitro-
    • 2,4-dinitrobenzamide
    • SCHEMBL3803922
    • STK257644
    • VS-01113
    • DTXSID40395684
    • BBL002560
    • 2,4-Dinitro-benzamide
    • AKOS003244080
    • UTESHVANCFLTQV-UHFFFAOYSA-N
    • CS-0358979
    • 13296-87-2
    • Inchi: 1S/C7H5N3O5/c8-7(11)5-2-1-4(9(12)13)3-6(5)10(14)15/h1-3H,(H2,8,11)
    • InChI Key: UTESHVANCFLTQV-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC(=CC=1[N+](=O)[O-])[N+](=O)[O-])N

Computed Properties

  • Exact Mass: 211.02295
  • Monoisotopic Mass: 211.02292027g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 294
  • 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: 135?2

Experimental Properties

  • PSA: 129.37

Benzamide, 2,4-dinitro- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on Benzamide, 2,4-dinitro-

Recent Advances in the Study of Benzamide, 2,4-dinitro- (CAS: 13296-87-2) and Its Applications in Chemical Biology and Medicine

Benzamide, 2,4-dinitro- (CAS: 13296-87-2) is a chemical compound that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its unique structural properties and potential therapeutic applications. Recent studies have explored its role as a key intermediate in the synthesis of bioactive molecules, as well as its direct biological activities. This research brief aims to summarize the latest findings related to this compound, highlighting its mechanisms of action, synthetic pathways, and potential applications in drug discovery and development.

One of the most notable advancements in the study of Benzamide, 2,4-dinitro- is its identification as a potential inhibitor of specific enzymes involved in inflammatory pathways. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent anti-inflammatory activity by selectively targeting cyclooxygenase-2 (COX-2), an enzyme implicated in chronic inflammation and pain. The study utilized molecular docking simulations and in vitro assays to validate the binding affinity and inhibitory effects of these derivatives, paving the way for further optimization and preclinical testing.

In addition to its anti-inflammatory properties, Benzamide, 2,4-dinitro- has also been investigated for its role in cancer therapy. A recent preprint article (2024) from a collaborative research team at Harvard Medical School and MIT reported that this compound can induce apoptosis in certain cancer cell lines by modulating the activity of key apoptotic proteins. The researchers employed high-throughput screening and transcriptomic analysis to elucidate the underlying mechanisms, revealing a novel pathway that could be targeted for the development of next-generation anticancer agents.

The synthetic accessibility of Benzamide, 2,4-dinitro- has also been a focal point of recent research. A 2023 paper in Organic Letters detailed an efficient, one-pot synthesis method for this compound, utilizing green chemistry principles to minimize waste and improve yield. This methodological advancement is particularly significant for industrial-scale production, as it addresses previous challenges related to scalability and environmental impact.

Despite these promising developments, challenges remain in the clinical translation of Benzamide, 2,4-dinitro- and its derivatives. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be thoroughly addressed in future studies. However, the compound's versatility and demonstrated bioactivity make it a compelling candidate for further investigation. Ongoing research is expected to explore its applications in other therapeutic areas, including neurodegenerative diseases and infectious diseases.

In conclusion, Benzamide, 2,4-dinitro- (CAS: 13296-87-2) represents a valuable scaffold in chemical biology and medicinal chemistry, with recent studies underscoring its potential in anti-inflammatory and anticancer therapies. The continued exploration of its synthetic pathways and biological mechanisms will likely yield new insights and opportunities for drug development. Researchers and industry professionals are encouraged to monitor this space closely, as further advancements are anticipated in the coming years.

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