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Key Documents

D163708

Sigma-Aldrich

N,O-Dimethylhydroxylamine hydrochloride

98%

Synonym(s):

N,O-Dimethylhydroxylamine HCl, N-Methoxymethylamine hydrochloride, Methoxymethylamine hydrochloride

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About This Item

Linear Formula:
CH3ONHCH3 · HCl
CAS Number:
Molecular Weight:
97.54
Beilstein/REAXYS Number:
3650353
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

crystals

mp

112-115 °C

SMILES string

Cl[H].CNOC

InChI

1S/C2H7NO.ClH/c1-3-4-2;/h3H,1-2H3;1H

Inchi Key

USZLCYNVCCDPLQ-UHFFFAOYSA-N

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Application

Reagent for the preparation of Weinreb amides recently used in the synthesis of 2-acyloxazoles from 2-oxazolemagnesium chloride.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Daniel J Pippel et al.
The Journal of organic chemistry, 72(15), 5828-5831 (2007-06-26)
Treatment of oxazole or 5-aryl oxazoles with i-PrMgCl smoothly generates the corresponding 2-Grignard reagents, which react with Weinreb amides to provide exclusively 2-acyl oxazole products.

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