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
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关于此项目
线性分子式:
NH2CONHNH2 · HCl
化学文摘社编号:
分子量:
111.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-247-0
Beilstein/REAXYS Number:
3593642
MDL number:
产品名称
氨基脲 盐酸盐, ≥99%
InChI key
XHQYBDSXTDXSHY-UHFFFAOYSA-N
InChI
1S/CH5N3O.ClH/c2-1(5)4-3;/h3H2,(H3,2,4,5);1H
SMILES string
Cl.NNC(N)=O
assay
≥99%
mp
175-177 °C (dec.) (lit.)
Quality Level
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Application
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。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Oral
target_organs
Bone
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Experimental and theoretical evaluation of semicarbazones and thiosemicarbazones as organic corrosion inhibitors.
Goulart C M, et al.
Corrosion Science, 67, 281-291 (2013)
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 and antimicrobial activity of some novel derivatives of benzofuran: Part 2. The synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives.
Kirilmis C, et al.
European Journal of Medicinal Chemistry, 43(2), 300-308 (2008)
Semicarbazide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
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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