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S9757

Sigma-Aldrich

Sulfabenzamide

Synonym(s):

N-(4-Aminobenzenesulfonyl)benzamide, N-Sulfanilylbenzamide

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About This Item

Empirical Formula (Hill Notation):
C13H12N2O3S
CAS Number:
127-71-9
Molecular Weight:
276.31
Beilstein/REAXYS Number:
2139003
EC Number:
204-859-4
MDL number:
MFCD00044890
UNSPSC Code:
51101500
PubChem Substance ID:
24899854

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

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General description

Chemical structure: sulfonamide

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Nino G Todua et al.
Rapid communications in mass spectrometry : RCM, 25(6), 750-754 (2011-02-22)
Mono-, di- and trialkyl derivatives of 'sulfabenzamide' (N-4-aminophenylsulfonylbenzamide) have been prepared and their electron ionization (EI) mass spectra examined. It is found that the fragmentation of N-alkylsulfabenzamides (alkyl = CH(3) to n-C(5)H(11)) proceeds via a very specific rearrangement process. The proposed mechanism
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
[Physico-chemical comparison of two sulfamides: sulfaproxyline and sulfabenzamide].
L Maury et al.
Pharmaceutica acta Helvetiae, 62(4), 116-120 (1987-01-01)
C A Spinks et al.
Bioconjugate chemistry, 10(4), 583-588 (1999-07-20)
Molecular modeling of hapten structure was used to predict and influence, through appropriate synthetic work, the outcome of an immunization program. Examination of the structures of sulfonamide antibiotics led to the development of a hypothesis and the consequent synthesis of
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
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