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Merck

254568

Sigma-Aldrich

O-烯丙基羟胺 盐酸盐 水合物

97%

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About This Item

线性分子式:
H2C=CHCH2ONH2·HCl·xH2O
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

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.

象形图

Corrosion

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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