推荐产品
质量水平
检测方案
≥97.0% (CHN)
形式
solid
mp
85-89 °C (lit.)
SMILES字符串
CS(N)(=O)=O
InChI
1S/CH5NO2S/c1-5(2,3)4/h1H3,(H2,2,3,4)
InChI key
HNQIVZYLYMDVSB-UHFFFAOYSA-N
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应用
- 甲磺酰胺用于合成重要的有机试剂，如 N -（2-甲硫基-1- p -甲苯磺酰）甲磺酰胺和 叔 -丁基（（2-（三甲基硅基）乙基）磺酰基）氨基甲酸酯。
- 可作为氮源用于羧酸转化为相应的的腈。
- 它作为一种试剂被广泛用于合成药物上重要的化合物，如吲哚衍生物 N -乙酰胺 、甲磺酰胺嘧啶取代的 3,5-二羟基-6-庚烯酸类 和 repertaxin 。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
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
2-Arylpropionic CXC chemokine receptor 1 (CXCR1) ligands as novel noncompetitive CXCL8 inhibitors.
Allegretti M, et al.
Journal of Medicinal Chemistry, 48(13), 4312-4331 (2005)
Synthesis and biological activity of methanesulfonamide pyrimidine-and N-methanesulfonyl pyrrole-substituted 3, 5-dihydroxy-6-heptenoates, a novel series of HMG-CoA reductase inhibitors.
Watanabe M, et al.
Bioorganic & Medicinal Chemistry, 5(2), 437-444 (1997)
A Convenient Synthesis of Chloronitrobenzonitrile Isomers and Homologs.
Grivsky E M
Bull. Soc. Chim. Belg., 80(3?4), 245-252 (1971)
Development and preliminary optimization of indole-N-acetamide inhibitors of hepatitis C virus NS5B polymerase.
Harper S, et al.
Journal of Medicinal Chemistry, 48(5), 1314-1317 (2005)
T H Maren et al.
The Journal of biological chemistry, 268(35), 26233-26239 (1993-12-15)
Aliphatic sulfonamides, as CH3SO2NH2, are very weak inhibitors of the carbonic anhydrases (KI congruent to 10(-4) M) and are extremely weak acids (Ka congruent to 10(-10.5) M). We now find CF3SO2NH2 a very potent inhibitor of carbonic anhydrase II (KI
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