Cas no 94160-04-0 (Benzenesulfonamide,3-amino-4-chloro-N-phenyl-)

Benzenesulfonamide, 3-amino-4-chloro-N-phenyl-, is a specialized aromatic sulfonamide derivative characterized by its amino and chloro substituents on the benzene ring, along with an N-phenyl group. This compound is of interest in synthetic organic chemistry and pharmaceutical research due to its potential as an intermediate in the development of bioactive molecules. The presence of both electron-donating (amino) and electron-withdrawing (chloro) groups enhances its reactivity, making it suitable for further functionalization. Its structural features may also contribute to interactions with biological targets, particularly in the design of sulfonamide-based therapeutics. The compound is typically handled under controlled conditions due to its reactive functional groups.
Benzenesulfonamide,3-amino-4-chloro-N-phenyl- structure
94160-04-0 structure
Product Name:Benzenesulfonamide,3-amino-4-chloro-N-phenyl-
CAS No:94160-04-0
MF:C12H11ClN2O2S
MW:282.745940446854
CID:805809
PubChem ID:2873180
Update Time:2025-11-06

Benzenesulfonamide,3-amino-4-chloro-N-phenyl- Chemical and Physical Properties

Names and Identifiers

    • Benzenesulfonamide,3-amino-4-chloro-N-phenyl-
    • 3-Amino-4-chloro-N-phenylbenzenesulfonamide
    • 3-amino-4-chloro-N-phenylbenzenesulphonamide
    • SMSF0008620
    • CB09382
    • Benzenesulfonamide, 3-amino-4-chloro-N-phenyl-
    • AE-641/02492046
    • DTXSID40240887
    • 94160-04-0
    • BIM-0006913.P001
    • 3-AMINO-4-CHLORO-N-PHENYLBENZENE-1-SULFONAMIDE
    • CBMicro_007023
    • NS00093066
    • CS-0365872
    • UYN4XE4LDW
    • EINECS 303-285-2
    • SR-01000222015
    • SR-01000222015-1
    • AKOS005828184
    • SCHEMBL3320242
    • UNII-UYN4XE4LDW
    • SB82401
    • MDL: MFCD01911903
    • Inchi: 1S/C12H11ClN2O2S/c13-11-7-6-10(8-12(11)14)18(16,17)15-9-4-2-1-3-5-9/h1-8,15H,14H2
    • InChI Key: ZXDUBUVCNBHUHO-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=CC=1N)S(NC1C=CC=CC=1)(=O)=O

Computed Properties

  • Exact Mass: 282.022976
  • Monoisotopic Mass: 282.022976
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 363
  • 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
  • Topological Polar Surface Area: 80.6

Experimental Properties

  • Density: 1.466
  • Boiling Point: 462.9°Cat760mmHg
  • Flash Point: 233.7°C

Benzenesulfonamide,3-amino-4-chloro-N-phenyl- Security Information

  • HazardClass:IRRITANT

Benzenesulfonamide,3-amino-4-chloro-N-phenyl- Pricemore >>

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Additional information on Benzenesulfonamide,3-amino-4-chloro-N-phenyl-

Market Research Analysis of 3-Amino-4-Chloro-N-Phenylbenzenesulfonamide (CAS No. 94160-04-0) in Chemical-Biomedical Fields

The compound 3-Amino-4-Chloro-N-Phenylbenzenesulfonamide, identified by the CAS number 94160-04-0, has garnered significant attention in the chemical-biomedical industry due to its potential applications in drug development and therapeutic interventions. This analysis aims to provide a comprehensive overview of the current market landscape, research advancements, and future prospects of this compound.

Recent studies have highlighted the compound's role as a promising candidate in the development of novel therapeutic agents. Its unique chemical structure, characterized by the presence of amino and chloro substituents on the benzene ring, coupled with the sulfonamide group, endows it with distinctive pharmacological properties. These properties include enhanced bioavailability, improved stability, and potential bioactivity against various disease targets.

Market demand for 3-Amino-4-Chloro-N-Phenylbenzenesulfonamide has been driven by its application in preclinical studies targeting diseases such as cancer, inflammatory disorders, and infectious diseases. The compound's ability to modulate key biological pathways makes it a valuable asset in drug discovery pipelines.

Global suppliers have demonstrated increasing capacity to meet the rising demand for this compound. Key players in the market are focusing on optimizing production processes to ensure cost-effectiveness and scalability. Additionally, regulatory approvals and compliance with international standards have been critical factors influencing market dynamics.

Looking ahead, the market is expected to witness further growth as more research initiatives explore the therapeutic potential of this compound. Collaborative efforts between academia and industry are anticipated to accelerate its translation into clinical applications.

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