108146
Benzenesulfonamide
≥98%
Synonyme(s) :
Phenylsulfonamide
Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
About This Item
Formule linéaire :
C6H5SO2NH2
Numéro CAS:
Poids moléculaire :
157.19
Numéro Beilstein :
1100566
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
eCl@ss :
39093209
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
![1,4-Diazabicyclo[2.2.2]octane ReagentPlus®, ≥99%](/deepweb/assets/sigmaaldrich/product/structures/366/129/a6ff4175-974d-4fac-9038-b35e508ef252/640/a6ff4175-974d-4fac-9038-b35e508ef252.png)
Niveau de qualité
Pureté
≥98%
Forme
solid
Pf
149-152 °C (lit.)
Solubilité
methanol: soluble 25 mg/mL
Chaîne SMILES
NS(=O)(=O)c1ccccc1
InChI
1S/C6H7NO2S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H2,7,8,9)
Clé InChI
KHBQMWCZKVMBLN-UHFFFAOYSA-N
Informations sur le gène
human ... CA1(759)
Vous recherchez des produits similaires ? Visite Guide de comparaison des produits
Catégories apparentées
Application
Benzenesulfonamide was used to develop analytical method for simultaneous determination of benzotriazole, benzothiazole and benzenesulfonamide contaminants in environmental waters.
Actions biochimiques/physiologiques
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.
Notes préparatoires
Benzenesulfonamide dissolves in methanol at a concentration of 25 mg/ml to form a clear, colourless solution.
Mention d'avertissement
Warning
Mentions de danger
Classification des risques
Acute Tox. 4 Oral
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
Les clients ont également consulté
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
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
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
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
Nitrogen-15 nuclear magnetic resonance study of benzenesulfonamide and cyanate binding to carbonic anhydrase.
K Kanamori et al.
Biochemistry, 22(11), 2658-2664 (1983-05-24)
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
Contacter notre Service technique