Cas no 6933-51-3 (N-(2-nitrophenyl)benzenesulfonamide)

N-(2-Nitrophenyl)benzenesulfonamide is a sulfonamide derivative characterized by the presence of a nitro group at the ortho position of the phenyl ring. This compound is of interest in organic synthesis and pharmaceutical research due to its potential as an intermediate in the preparation of more complex molecules. The nitro group enhances reactivity, facilitating further functionalization, while the sulfonamide moiety offers stability and versatility in chemical transformations. Its well-defined structure and purity make it suitable for applications in medicinal chemistry, particularly in the development of bioactive compounds. The compound is typically handled under standard laboratory conditions, with attention to compatibility in reactions involving nucleophiles or reducing agents.
N-(2-nitrophenyl)benzenesulfonamide structure
6933-51-3 structure
Product Name:N-(2-nitrophenyl)benzenesulfonamide
CAS No:6933-51-3
MF:C12H10N2O4S
MW:278.283801555634
MDL:MFCD00193728
CID:973471
PubChem ID:285267
Update Time:2025-11-02

N-(2-nitrophenyl)benzenesulfonamide Chemical and Physical Properties

Names and Identifiers

    • N-(2-nitrophenyl)benzenesulfonamide
    • 2-nitro-1-phenylsulfonamidobenzene
    • 2'nitrobenzenesulfonanilide
    • 2'-Nitrobenzenesulfonanilide
    • 2'-Nitrobenzenesulphanilide
    • AC1L62PE
    • AC1Q6VY2
    • ARONIS004010
    • benzenesulfonamide, n-(2-nitrophenyl)-
    • N-(2-nitrophenyl)phenylsulfonamide
    • N-(4-chloro-2-nitrophenyl)benzenesulfonamide
    • N-phenylsulfonyl-2-nitroaniline
    • NSC142099
    • SureCN2003165
    • CHEMBL448843
    • SCHEMBL2003165
    • EU-0036325
    • NSC-142099
    • MLS002920542
    • QYEQJQLZLZRQEB-UHFFFAOYSA-N
    • N-(2-Nitrophenyl)benzenesulfonamide #
    • DTXSID50301256
    • SB81790
    • LS-07447
    • MFCD00193728
    • SMR001798131
    • AKOS000493657
    • 6933-51-3
    • STK090834
    • DS-001838
    • MDL： MFCD00193728
    • Inchi： 1S/C12H10N2O4S/c15-14(16)12-9-5-4-8-11(12)13-19(17,18)10-6-2-1-3-7-10/h1-9,13H
    • InChI Key： QYEQJQLZLZRQEB-UHFFFAOYSA-N
    • SMILES： S(C1C=CC=CC=1)(NC1C=CC=CC=1[N+](=O)[O-])(=O)=O

Computed Properties

  • Exact Mass: 278.0362
  • Monoisotopic Mass: 278.036
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 3
  • Complexity: 406
  • 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: 2.8
  • Topological Polar Surface Area: 100A^2

Experimental Properties

  • Density: 1.461
  • Boiling Point: 451.3°C at 760 mmHg
  • Flash Point: 226.8°C
  • Refractive Index: 1.656
  • PSA: 89.31
  • LogP: 4.07260

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N-(2-nitrophenyl)benzenesulfonamide Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:6933-51-3)N-(2-nitrophenyl)benzenesulfonamide
Order Number:A1172189
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 01:22
Price ($):264.0

N-(2-nitrophenyl)benzenesulfonamide Related Literature

Additional information on N-(2-nitrophenyl)benzenesulfonamide

Comprehensive Analysis of N-(2-nitrophenyl)benzenesulfonamide (CAS No. 6933-51-3)

N-(2-nitrophenyl)benzenesulfonamide (CAS No. 6933-51-3) is a sulfonamide derivative with significant applications in organic synthesis and pharmaceutical research. This compound, characterized by its nitrophenyl and benzenesulfonamide functional groups, has garnered attention due to its unique chemical properties and potential industrial uses. Researchers and manufacturers often seek information on its synthesis, stability, and reactivity, making it a trending topic in chemical databases and academic discussions.

The molecular structure of N-(2-nitrophenyl)benzenesulfonamide features a sulfonamide linkage (-SO2NH-) bridging a benzene ring and a 2-nitrophenyl group. This configuration contributes to its moderate polarity, making it soluble in organic solvents like dimethyl sulfoxide (DMSO) and acetone. Its nitro group (-NO2) enhances its electron-withdrawing properties, which is critical in designing catalysts or intermediates for agrochemicals and dyes. Recent studies highlight its role in green chemistry initiatives, where safer alternatives to traditional reagents are explored.

In the context of drug discovery, N-(2-nitrophenyl)benzenesulfonamide is investigated for its potential as a pharmacophore. Sulfonamides are known for their antibacterial and anti-inflammatory properties, and modifications to the nitrophenyl moiety could unlock novel therapeutic applications. Questions like "How does N-(2-nitrophenyl)benzenesulfonamide interact with enzymes?" or "What are its biodegradation pathways?" are frequently searched in academic and industrial forums, reflecting its relevance in biochemical research.

From an industrial perspective, this compound is valued for its role in high-performance material synthesis. Its thermal stability and compatibility with polymers make it a candidate for advanced coatings or adhesives. Environmental concerns have also driven interest in its eco-friendly derivatives, aligning with global trends toward sustainable chemistry. Searches for "CAS 6933-51-3 supplier" or "benzenesulfonamide safety data" indicate strong market demand and regulatory awareness.

Analytical techniques such as HPLC, NMR spectroscopy, and mass spectrometry are essential for characterizing N-(2-nitrophenyl)benzenesulfonamide. Purity assessments and impurity profiling are critical for compliance with Good Manufacturing Practices (GMP), especially when used in pharmaceutical intermediates. The compound’s UV absorption properties also make it suitable for spectroscopic applications, a feature often queried in research databases.

In summary, N-(2-nitrophenyl)benzenesulfonamide (CAS No. 6933-51-3) exemplifies the intersection of organic chemistry and applied science. Its versatility in synthesis, material science, and drug development ensures its continued relevance. As industries prioritize sustainability and innovation, this compound will likely remain a focal point for scientific and commercial exploration.

6933-51-3 (N-(2-nitrophenyl)benzenesulfonamide) Related Products

Recommended suppliers
Amadis Chemical Company Limited
(CAS:6933-51-3)N-(2-nitrophenyl)benzenesulfonamide
A1172189
Purity:99%
Quantity:1g
Price ($):264.0
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