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Merck
CN

211370

Sigma-Aldrich

磺酰胺

99%

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别名:
Imidosulfamic acid, Sulfamoylamine, Sulfonyl diamide, Sulfuryl amide, Sulfuryl diamide
线性分子式:
(NH2)2SO2
CAS号:
分子量:
96.11
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

mp

90-92 °C (lit.)

溶解性

water: soluble 50 mg/mL, clear, colorless to faintly yellow

密度

1.611 g/mL at 25 °C (lit.)

SMILES字符串

NS(N)(=O)=O

InChI

1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)

InChI key

NVBFHJWHLNUMCV-UHFFFAOYSA-N

基因信息

human ... CA1(759) , CA2(760)

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一般描述

磺酰胺,一种与格氏试剂相容的极性非质子溶剂,可用作医学化学中的官能团。

应用

磺胺被用于合成以下物质:
  • ArCH=NSO2NH2型席夫碱
  • 1H,3H-2,1,3-苯并噻二嗪-4-酮-2,2-二氧化物(BTDD)
  • 在一项PPARα激活的研究中,合成油酰乙醇胺类似物的磺酰胺类似物。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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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Anomeric effects in sulfamides
Eric H et al.
The Journal of Physical Chemistry A, 120, 3677-3682 (2016)
Sulfamides and sulfonamides as polar aprotic solvents
Herman R G et al.
The Journal of Organic Chemistry, 52, 479-483 (1987)
Anthony Bertucci et al.
Bioorganic & medicinal chemistry letters, 19(3), 650-653 (2009-01-06)
The inhibition of a coral carbonic anhydrase (CA, EC 4.2.1.1) has been investigated with a series of inorganic anions such as halogenides, pseudohalogenides, bicarbonate, carbonate, nitrate, nitrite, hydrogen sulfide, bisulfite, perchlorate, sulfate. The full-length scleractinian coral Stylophora pistillata CA, STPCA
Jean-Yves Winum et al.
Bioorganic & medicinal chemistry letters, 15(9), 2353-2358 (2005-04-20)
A small library of N-hydroxysulfamides was synthesized by an original approach in order to investigate whether this zinc-binding function is efficient for the design of inhibitors targeting the cytosolic (hCA I and II) and transmembrane, tumor-associated (hCA IX and XII)
A Scozzafava et al.
Journal of enzyme inhibition, 15(5), 443-453 (2000-10-13)
Sulfamide and sulfamic acid are the simplest compounds containing the SO2NH2 moiety, responsible for binding to the Zn(II) ion within carbonic anhydrase (CA, EC 4.2.1.1) active site, and thus acting as inhibitors of the many CA isozymes presently known. Here

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