N-Methoxy-N-methylacetamide

N-Methoxy-N-methylacetamide Basic information

Product Name:	N-Methoxy-N-methylacetamide
Synonyms:	N-METHOXY-N-METHYLACETAMIDE;N-METHOXY-N-METHLACETAMIDE;N-Methoxy-N-methylacetamide, 98 %;AcetaMide, N-Methoxy-N-Methyl-;N-Methoxy-N-MethylacetaMide, 95+%;N-Methoxy-N-methylacetamide;N-Methyl-N-methoxyacetamide;N-Methoxyl-N-methylacetamide
CAS:	78191-00-1
MF:	C4H9NO2
MW:	103.12
EINECS:	628-920-3
Product Categories:	Hydroxylamines;Hydroxylamines (N-Substituted);Hydroxylamines (O-Substituted);Amides;Carbonyl Compounds;Organic Building Blocks;bc0001
Mol File:	78191-00-1.mol

N-Methoxy-N-methylacetamide Chemical Properties

Boiling point	152 °C (lit.)
density	0.97 g/mL at 25 °C (lit.)
refractive index	n20/D 1.426(lit.)
Fp	121 °F
storage temp.	Inert atmosphere,Room Temperature
solubility	Chloroform (Slightly), Methanol (Slightly)
form	Liquid
color	Colorless
Water Solubility	Soluble
CAS DataBase Reference	78191-00-1(CAS DataBase Reference)

Safety Information

Risk Statements	10
Safety Statements	16-24/25
RIDADR	UN 1993 3/PG 3
WGK Germany	3
HazardClass	3
PackingGroup	III
HS Code	29280000

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English

N-Methoxy-N-methylacetamide Usage And Synthesis

Chemical Properties	clear colorless liquid
Uses	N-Methoxy-N-methylacetamide, is a Weinreb amide used in the synthesis of marine natural products myriaporone and usneoidone as a ketone synthon.
General Description	Simple Weinreb amide used in the synthesis of marine natural products myriaporone and usneoidone as a ketone synthon.

N-Methoxy-N-methylacetamide Preparation Products And Raw materials

Raw materials	Acetonoxim-o-methylether-->2-CHLORO-N-METHOXY-N-METHYLACETAMIDE-->Trifluoroacetophenone-->N-methoxymethylamine-->N,O-Dimethylhydroxylamine hydrochloride-->1,4-Cyclohexanedione
Preparation Products	1-(4-FLUORO-PHENYL)-BUT-3-EN-2-ONE-->3'-BroMo-5'-(trifluoroMethyl)acetophenone, 97%-->3-HEXYN-2-ONE-->1-(5-Bromo-2,4-difluoro-phenyl)-ethanone-->5-BROMO-2-METHYL-1H-BENZIMIDAZOLE-->5-ACETYL-2-METHOXYPYRIDINE, 97%-->5-Acetylindole-->1-(6-chloro-2-methoxypyridin-3-yl)ethanone-->1-(2-CHLORO-3-FLUOROPYRIDIN-4-YL)ETHANONE

2-(3-FLUOROPHENYL)-N-METHOXY-N-METHYLACETAMIDE 3-Maleimidobenzoic acid N-hydroxysuccinimide ester 2-[(2,6-DICHLOROPYRIDIN-4-YL)THIO]-N-METHOXY-N-METHYLACETAMIDE (2-NAPHTHOXY)ACETIC ACID N-HYDROXYSUCCINIMIDE ESTER SPDP CARBONIC ACID TERT-BUTYL PHTHALIMIDO ESTER Methoxy N-(2-carbamothioylethyl)-2-methoxy-N-methylacetamide N-HYDROXYSUCCINIMIDYL ACETOACETATE N-Succinimidyl S-Acetylthioglycolate DI(N-SUCCINIMIDYL) OXALATE 2-(3,4-dichlorophenyl)-N-methoxy-N-methylacetamide 2-[(4-aminophenyl)methoxy]-N-methylacetamide N-(2-Chlorobenzyloxycarbonyloxy)succinimide 5(6)-CARBOXY-2',7'-DICHLOROFLUORESCEIN DIACETATE N-SUCCINIMIDYL ESTER BOC-TRP-OSU BOC-ILE-OSU 2-(BENZYLOXY)-1H-ISOINDOLE-1,3(2H)-DIONE

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