Cas no 10475-06-6 (5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide)

5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide is a sulfonamide derivative characterized by its amino and chloro substituents on the benzene ring, along with a dimethylated sulfonamide functional group. This compound is of interest in synthetic organic chemistry due to its potential as an intermediate in pharmaceutical and agrochemical applications. The presence of both electron-donating (amino) and electron-withdrawing (chloro, sulfonamide) groups enhances its reactivity in electrophilic and nucleophilic substitution reactions. Its structural features make it suitable for further functionalization, enabling the synthesis of more complex molecules. The compound is typically handled under controlled conditions due to its sensitivity to moisture and light. Analytical methods such as HPLC and NMR are recommended for purity assessment.
5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide structure
10475-06-6 structure
Product Name:5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide
CAS No:10475-06-6
MF:C8H11ClN2O2S
MW:234.703139543533
CID:226488
PubChem ID:3613938
Update Time:2025-05-19

5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide Chemical and Physical Properties

Names and Identifiers

    • 5-Amino-2-chloro-N,N-dimethylbenzenesulfonamide
    • 5-AMINO-2-CHLORO-N,N-DIMETHYL-BENZENESULFONAMIDE
    • Benzenesulfonamide,5-amino-2-chloro-N,N-dimethyl-
    • AC1MU7G8
    • AC1Q3WZA
    • CTK4A3285
    • N,N,-dimethyl-5-amino-2-chlorobenzenesulfonamide
    • N,N-dimethyl-2-chloro-5-aminobenzene-sulfonamide
    • SureCN8936354
    • AKOS000115643
    • Z56779172
    • ODCHLWPLEOVWHX-UHFFFAOYSA-N
    • MFCD02700603
    • SR-01000027742-1
    • N,N-dimethyl-2-chloro-5-aminobenzenesulfonamide
    • SB80618
    • DTXSID60394250
    • SCHEMBL8936354
    • 10475-06-6
    • AT13553
    • EN300-02144
    • SR-01000027742
    • BS-25566
    • 5-amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide
    • 5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide
    • Inchi: 1S/C8H11ClN2O2S/c1-11(2)14(12,13)8-5-6(10)3-4-7(8)9/h3-5H,10H2,1-2H3
    • InChI Key: ODCHLWPLEOVWHX-UHFFFAOYSA-N
    • SMILES: ClC1=CC=C(C=C1S(N(C)C)(=O)=O)N

Computed Properties

  • Exact Mass: 234.02313
  • Monoisotopic Mass: 234.0229765g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 286
  • 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
  • Topological Polar Surface Area: 71.8?2

Experimental Properties

  • PSA: 63.4

5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide Pricemore >>

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Additional information on 5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide

Comprehensive Overview of 5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide (CAS No. 10475-06-6)

5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide, identified by its CAS No. 10475-06-6, is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. This sulfonamide derivative features a unique molecular structure, combining an amino group, a chloro substituent, and a dimethylsulfonamide moiety, making it a versatile intermediate in synthetic chemistry. Researchers and industry professionals frequently search for terms like "sulfonamide applications", "chlorobenzene derivatives", and "amino-functionalized sulfonamides" to explore its potential.

The compound’s significance has grown alongside advancements in drug discovery and material science. Recent trends highlight its role in developing enzyme inhibitors and antimicrobial agents, addressing global concerns like antibiotic resistance. Searches for "sulfonamide-based therapeutics" and "green synthesis of chlorinated compounds" reflect rising interest in sustainable methodologies. Its stability under varied pH conditions also makes it a candidate for catalysis research and high-performance polymer development.

From a structural perspective, the 5-amino-2-chloro configuration enhances reactivity in electrophilic substitutions, while the N,N-dimethylsulfonamide group improves solubility in organic solvents. This balance is critical for applications in heterocyclic synthesis, a topic frequently queried as "building blocks for medicinal chemistry". Analytical techniques such as HPLC and NMR spectroscopy are commonly employed to characterize its purity, aligning with search terms like "sulfonamide analysis methods".

Environmental and safety considerations are also paramount. While not classified as hazardous, proper handling protocols are emphasized in queries like "safe storage of sulfonamides". The compound’s biodegradability and low toxicity profile align with the green chemistry movement, a trending topic in scientific communities. Researchers often explore "eco-friendly sulfonamide derivatives" to minimize ecological impact.

In summary, 5-Amino-2-chloro-N,N-dimethylbenzene-1-sulfonamide (CAS 10475-06-6) bridges multiple disciplines, from pharmaceuticals to advanced materials. Its adaptability to modern challenges, such as sustainable synthesis and drug design, ensures its relevance in ongoing scientific discourse. For further details, keywords like "sulfonamide reactivity" and "chloro-amino benzene applications" can deepen understanding of this compound’s multifaceted role.

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