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About This Item
Linear Formula:
H2C=CHCH2ONH2·HCl·xH2O
CAS Number:
Molecular Weight:
109.55 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
175 °C (dec.) (lit.)
solubility
methanol: soluble 25 mg/mL, clear, colorless
SMILES string
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
Application
O-Allylhydroxylamine hydrochloride hydrate has been used in the preparation of acetophenone O-allyloxime and O-allyI-N-(2-trimethylsilylethyloxycarbonyl)-hydroxylamine.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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)
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
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