S2201
氨基脲 盐酸盐
≥99%
别名:
N-氨基脲 盐酸盐, 氨基甲酰肼 盐酸盐
质量水平
方案
≥99%
mp
175-177 °C (dec.) (lit.)
SMILES字符串
Cl.NNC(N)=O
InChI
1S/CH5N3O.ClH/c2-1(5)4-3;/h3H2,(H3,2,4,5);1H
InChI key
XHQYBDSXTDXSHY-UHFFFAOYSA-N
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应用
氨基脲盐酸盐是用于从醛和酮合成缩氨基脲的通用试剂。可用于构建多种杂环化合物,其中一些是有效的抗菌剂和抗病毒剂。也可用于制备阻蚀剂。
醛和酮的衍生试剂,其可产生具有特征熔点的结晶化合物。
警示用语:
Danger
危险分类
Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Oral
靶器官
Bone
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Semicarbazide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Experimental and theoretical evaluation of semicarbazones and thiosemicarbazones as organic corrosion inhibitors.
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Kirilmis C, et al.
European Journal of Medicinal Chemistry, 43(2), 300-308 (2008)
Design, synthesis, and biological evaluation of antiviral agents targeting flavivirus envelope proteins.
Li Z, et al.
Journal of Medicinal Chemistry, 51(15), 4660-4671 (2008)
Synthesis of some new azole, azepine, pyridine, and pyrimidine derivatives using 6?hydroxy?4H?4?oxo [1]?benzopyran?3?carboxaldehyde as a versatile starting material.
Abdel?Rahman A H, et al.
Heteroatom Chem., 16(1), 20-27 (2005)
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