108146
Benzenesulfonamide
≥98%
Synonyme(s) :
Phenylsulfonamide
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A propos de cet article
Formule linéaire :
C6H5SO2NH2
Numéro CAS:
Poids moléculaire :
157.19
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39093209
UNSPSC Code:
12352100
EC Number:
202-637-1
MDL number:
Beilstein/REAXYS Number:
1100566
Assay:
≥98%
Form:
solid
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Laissez-nous vous aiderInChI key
KHBQMWCZKVMBLN-UHFFFAOYSA-N
InChI
1S/C6H7NO2S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H2,7,8,9)
SMILES string
NS(=O)(=O)c1ccccc1
assay
≥98%
form
solid
Quality Level
Gene Information
human ... CA1(759)
solubility
methanol: soluble 25 mg/mL
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Catégories apparentées
Application
Benzenesulfonamide was used to develop analytical method for simultaneous determination of benzotriazole, benzothiazole and benzenesulfonamide contaminants in environmental waters.
Biochem/physiol Actions
Benzenesulfonamide is an inhibitor of human carbonic anhydrase B. Benzenesulfonamide derivatives are effective in the treatment of proliferative diseases such as cancer. It is used in the synthesis of dyes, photochemicals and disinfectants.
Preparation Note
Benzenesulfonamide dissolves in methanol at a concentration of 25 mg/ml to form a clear, colourless solution.
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Astrid Goubet et al.
Bioorganic & medicinal chemistry letters, 23(3), 761-763 (2012-12-26)
C5-Ethynylbenzenesulfonamide-modified nucleotide (EBNA) was investigated as substrate of various DNA polymerases. The experiments revealed that KOD, Phusion and Klenow DNA polymerases successfully accepted EBNA-T nucleotide as a substrate and yielded the fully extended DNA. KOD DNA polymerase was found to
Asha Chandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 92, 84-90 (2012-03-27)
The FT-IR and FT-Raman spectra of (E)-N-carbamimidoyl-4-((4-methoxybenzylidene)amino)benzenesulfonamide were recorded and analyzed. Geometry and harmonic vibrational wavenumbers were calculated theoretically using Gaussian 03 set of quantum chemistry codes. Calculations were performed at the Hartree-Fock (HF) and density functional theory (DFT) levels
Rafia Bashir et al.
Bioorganic & medicinal chemistry letters, 21(14), 4301-4305 (2011-06-15)
Thirteen new 2-pyrazoline derivatives bearing benzenesulfonamide moiety (2a-m) were synthesized by condensing appropriate chalcones with 4-hydrazinonbenzenesulfonamide hydrochloride and tested for anticancer and anti-inflammatory actions. According to the protocol of the National Cancer Institute (NCI) in vitro disease-oriented human cells screening
Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases.
Edita Čapkauskaitė et al.
European journal of medicinal chemistry, 51, 259-270 (2012-03-24)
A series of [(2-pyrimidinylthio)acetyl]benzenesulfonamides were designed and synthesized. Their binding affinities as inhibitors of several recombinant human carbonic anhydrase (CA) isozymes were determined by isothermal titration calorimetry (ITC) and thermal shift assay (TSA). A group of compounds containing a chlorine
Theres Ramenda et al.
Amino acids, 44(4), 1167-1180 (2013-01-12)
Cu(I)-mediated [3+2]cycloaddition between azides and alkynes has evolved into a valuable bioconjugation tool in radiopharmaceutical chemistry. We have developed a simple, convenient and reliable radiosynthesis of 4-[18F]fluoro-N-methyl-N-(propyl-2-yn-1-yl)benzenesulfonamide ([18F]F-SA) as a novel aromatic sulfonamide-based click chemistry building block. [18F]F-SA could be
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