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Merck
CN

108146

Sigma-Aldrich

苯磺酰胺

≥98%

别名:

Phenylsulfonamide

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About This Item

线性分子式:
C6H5SO2NH2
CAS号:
分子量:
157.19
Beilstein:
1100566
EC 号:
MDL编号:
UNSPSC代码:
12352100
eCl@ss:
39093209
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥98%

形式

solid

mp

149-152 °C (lit.)

溶解性

methanol: soluble 25 mg/mL

SMILES字符串

NS(=O)(=O)c1ccccc1

InChI

1S/C6H7NO2S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H2,7,8,9)

InChI key

KHBQMWCZKVMBLN-UHFFFAOYSA-N

基因信息

human ... CA1(759)

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应用

苯磺酰胺被用于开发同时测定环境水中苯并三唑、苯并噻唑和苯磺酰胺污染物的分析方法

生化/生理作用

苯磺酰胺是人碳酸酐酶 B 的抑制剂 。苯磺酰胺衍生物对治疗癌症等增殖性疾病有效 。用于合成染料、光化学物和消毒剂

制备说明

苯磺酰胺溶于甲醇,浓度为 25 mg/mL,形成澄清、无色溶液。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Nitrogen-15 nuclear magnetic resonance study of benzenesulfonamide and cyanate binding to carbonic anhydrase.
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Biochemistry, 22(11), 2658-2664 (1983-05-24)
Yousuke Takaoka et al.
Chemical communications (Cambridge, England), 49(27), 2801-2803 (2013-02-27)
Here we describe how a (19)F-probe incorporated into an endogenous protein by a chemical biology method revealed protein dynamics. By explicit determination of ligand-bound and unbound structures with X-ray crystallography, the quantitative comparison of the protein's dynamics in live cells
Theres Ramenda et al.
Amino acids, 44(4), 1167-1180 (2013-01-12)
Cu(I)-mediated [3+2]cycloaddition between azides and alkynes has evolved into a valuable bioconjugation tool in radiopharmaceutical chemistry. We have developed a simple, convenient and reliable radiosynthesis of 4-[18F]fluoro-N-methyl-N-(propyl-2-yn-1-yl)benzenesulfonamide ([18F]F-SA) as a novel aromatic sulfonamide-based click chemistry building block. [18F]F-SA could be
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Journal of medicinal chemistry, 56(2), 510-520 (2012-12-14)
Carbonic anhydrase IX (CA-IX) is upregulated in cancer in response to the hypoxic tumor microenvironment, making it an attractive molecular target for the detection of hypoxic solid tumors. A series of small molecule benzenesulfonamide based CA-IX inhibitors containing novel tridentate
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Bioorganic & medicinal chemistry, 20(17), 5254-5261 (2012-07-27)
The P2Y(1) receptor (P2Y(1)R) is a G protein-coupled receptor naturally activated by extracellular ADP. Its stimulation is an essential requirement of ADP-induced platelet aggregation, thus making antagonists highly sought compounds for the development of antithrombotic agents. Here, through a virtual

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