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About This Item
Linear Formula:
CH3ONH2 · HCl
CAS Number:
Molecular Weight:
83.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-798-7
Beilstein/REAXYS Number:
3589723
MDL number:
Assay:
98%
Form:
solid
assay
98%
form
solid
mp
151-154 °C (lit.)
solubility
alcohol: soluble(lit.), water: soluble(lit.)
SMILES string
Cl.CON
InChI
1S/CH5NO.ClH/c1-3-2;/h2H2,1H3;1H
InChI key
XNXVOSBNFZWHBV-UHFFFAOYSA-N
General description
Methoxyamine hydrochloride combines with human antithrombin III-thrombin complex to form an inactive thrombin.
Application
Methoxyamine hydrochloride was used as a reagent in the preparation of O-methyl oximes. It was also used in the synthesis of O-methyl oximes from aldehydes or ketones.
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
flash_point_f
No data available
flash_point_c
No data available
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Tetrahedron Letters, 47, 6045-6045 (2006)
Edouard Godineau et al.
Organic letters, 8(21), 4871-4874 (2006-10-06)
[reaction: see text] A formal [2+2+2] process has been devised that allows the stereocontrolled formation of ring-fused piperidines from allylsilanes possessing an oxime moiety. The cascade involves an intermolecular radical addition of an alpha-iodoacetate onto an allylsilane double bond, which
Synthesis, 849-849 (1992)



