Merck
CN
所有图片(1)

文件

46762

Supelco

苯酰磺胺

VETRANAL®, analytical standard

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别名:
N-(4-氨基苯磺酰)苯甲酰胺
经验公式（希尔记法）:
C13H12N2O3S
CAS号:
127-71-9
分子量:
276.31
Beilstein:
2139003
EC 号:
204-859-4
MDL编号:
MFCD00044890
PubChem化学物质编号:
329757239
NACRES:
NA.24

等级

analytical standard

质量水平

200

产品线

VETRANAL®

保质期

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

clinical testing

格式

neat

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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相关类别

一般描述

Chemical structure: sulfonamide

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

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)
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
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
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
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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