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254568

Sigma-Aldrich

O-Allylhydroxylamine hydrochloride hydrate

97%

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About This Item

Linear Formula:
H2C=CHCH2ONH2·HCl·xH2O
CAS Number:
206557-03-1
Molecular Weight:
109.55 (anhydrous basis)
EC Number:
254-203-6
MDL number:
MFCD00150102
UNSPSC Code:
12352100
PubChem Substance ID:
24855393
NACRES:
NA.22
Assay:
97%

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[1] and O-allyI-N-(2-trimethylsilylethyloxycarbonyl)-hydroxylamine[2].

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

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Certificates of Analysis (COA)

Lot/Batch Number
S38078
22815PA
12618MQ
06213HQ
14328CN

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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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