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S9757

Sulfabenzamide

Name: Sulfabenzamide
Brand: SIGMA

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):

C₁₃H₁₂N₂O₃S

Número de CAS:

127-71-9

Peso molecular:

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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[Physico-chemical comparison of two sulfamides: sulfaproxyline and sulfabenzamide].

L Maury et al.

Pharmaceutica acta Helvetiae, 62(4), 116-120 (1987-01-01)

Electron ionization mass spectra of alkylated sulfabenzamides.

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

A systematic study on hydrogen bond interactions in sulfabenzamide: DFT calculations of the N-14, O-17, and H-2 NQR parameters.

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

In vitro susceptibility of Gardnerella vaginalis and Bacteroides organisms, associated with nonspecific vaginitis, to sulfonamide preparations.

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

Molecular modeling of hapten structure and relevance to broad specificity immunoassay of sulfonamide antibiotics.

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

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