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About This Item
线性分子式:
H2C=CHCH2ONH2·HCl·xH2O
CAS号:
分子量:
109.55 (anhydrous basis)
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
mp
175 °C (dec.) (lit.)
溶解性
methanol: soluble 25 mg/mL, clear, colorless
SMILES字符串
Cl[H].[H]O[H].NOCC=C
InChI
1S/C3H7NO.ClH.H2O/c1-2-3-5-4;;/h2H,1,3-4H2;1H;1H2
InChI key
VYCHJEXJHFTAQI-UHFFFAOYSA-N
应用
O-Allylhydroxylamine hydrochloride hydrate has been used in the preparation of acetophenone O-allyloxime and O-allyI-N-(2-trimethylsilylethyloxycarbonyl)-hydroxylamine.
警示用语:
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive 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 P3 (EN 143) respirator cartridges
J H van Maarseveen et al.
Bioorganic & medicinal chemistry, 5(5), 955-970 (1997-05-01)
In a search for the minimum pharmacophore of the naturally occurring tetracyclic eudistomins, five structural analogues (4-8) were evaluated for their in vitro antiviral and tumor cell antiproliferative activities. For the synthesis of these derivatives both intra- and intermolecular Pictet-Spengler
Synthesis of (R)-{η 6-[O-methyl-N-(α-methylbenzyl) hydroxyamino] benzene} chromium tricarbonyl via nucleophilic aromatic substitution of (η 6-fluorobenzene) chromium tricarbonyl.
da Costa MRG, et al.
Journal of the Chemical Society. Perkin Transactions 1, 21, 2850-2855 (2001)
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