S9757
Sulfabenzamide
Synonym(s):
N-(4-Aminobenzenesulfonyl)benzamide, N-Sulfanilylbenzamide
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About This Item
Empirical Formula (Hill Notation):
C13H12N2O3S
CAS Number:
Molecular Weight:
276.31
EC Number:
204-859-4
UNSPSC Code:
51101500
PubChem Substance ID:
Beilstein/REAXYS Number:
2139003
MDL number:
antibiotic activity spectrum
Gram-negative bacteria
storage temp.
2-8°C
SMILES string
Nc1ccc(cc1)S(=O)(=O)NC(=O)c2ccccc2
InChI
1S/C13H12N2O3S/c14-11-6-8-12(9-7-11)19(17,18)15-13(16)10-4-2-1-3-5-10/h1-9H,14H2,(H,15,16)
InChI key
PBCZLFBEBARBBI-UHFFFAOYSA-N
General description
Chemical structure: sulfonamide
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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B M Jones et al.
Antimicrobial agents and chemotherapy, 21(6), 870-872 (1982-06-01)
Recent reports suggest that anaerobic Bacteroides organisms are frequently found with Gardnerella vaginalis in nonspecific vaginitis. Specimens taken from 96 women with vaginal discharge were tested simultaneously for these organisms. G. vaginalis was found in 73% of the specimens, Bacteroides
Ahmad G Nozad et al.
Biophysical chemistry, 139(2-3), 116-122 (2008-11-26)
A systematic computational study was carried out to characterize the hydrogen bond, HB, interactions of sulfabenzamide crystal structure by DFT calculations of electric field gradient, EFG, tensors at the sites of 14N, 17O, and 2H nuclei. The computations were performed
[Physico-chemical comparison of two sulfamides: sulfaproxyline and sulfabenzamide].
L Maury et al.
Pharmaceutica acta Helvetiae, 62(4), 116-120 (1987-01-01)