226904
Methoxyamine hydrochloride
98%
동의어(들):
O-Methylhydroxylamine hydrochloride, Methoxylamine hydrochloride
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3ONH2 · HCl
CAS 번호:
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.
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
저장 등급
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
문서
DNA damage and repair mechanism is vital for maintaining DNA integrity. Damage to cellular DNA is involved in mutagenesis, the development of cancer among others.
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)