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:
Assay:
≥99%
Quality Level
assay
≥99%
mp
175-177 °C (dec.) (lit.)
SMILES string
Cl.NNC(N)=O
InChI
1S/CH5N3O.ClH/c2-1(5)4-3;/h3H2,(H3,2,4,5);1H
InChI key
XHQYBDSXTDXSHY-UHFFFAOYSA-N
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。
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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
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)
Experimental and theoretical evaluation of semicarbazones and thiosemicarbazones as organic corrosion inhibitors.
Goulart C M, et al.
Corrosion Science, 67, 281-291 (2013)
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| S2201-5G | 04061836918194 |
| S2201-500G | 04061836917951 |
| S2201-100G | 04061836917920 |