211370
磺酰胺
99%
别名:
磺酰二胺, 磺酰胺, 酰亚胺氨基磺酸
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关于此项目
线性分子式:
(NH2)2SO2
化学文摘社编号:
分子量:
96.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
232-262-9
MDL number:
产品名称
磺酰胺, 99%
InChI key
NVBFHJWHLNUMCV-UHFFFAOYSA-N
InChI
1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)
SMILES string
NS(N)(=O)=O
assay
99%
mp
90-92 °C (lit.)
solubility
water: soluble 50 mg/mL, clear, colorless to faintly yellow
density
1.611 g/mL at 25 °C (lit.)
Quality Level
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Application
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。
General description
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。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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)
Bacterial cleavage of nitrogen to sulfone bonds in sulfamide and 1H-2, 1, 3-benzothiadiazin-4 (3H)-one 2, 2-dioxide: formation of 2-nitrobenzamide by Gordonia sp.
Rein U and Cook AM.
FEMS Microbiology Letters, 172(2), 107-113 (1999)
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
Anna Di Fiore et al.
Bioorganic & medicinal chemistry letters, 20(12), 3601-3605 (2010-05-18)
We investigated the inhibition of carbonic anhydrase (CA, EC 4.2.1.1) isoforms I-XV with 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylsulfamide and other simple or sugar sulfamides, a class of less investigated CA inhibitors (CAIs). The crystal structure of the adduct of hCA II with the boron-substituted
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