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6919-61-5

6919-61-5 Structure

6919-61-5 Structure
IdentificationBack Directory
[Name]

N-METHOXY-N-METHYLBENZAMIDE
[CAS]

6919-61-5
[Synonyms]

N-Methyl-N-methoxybenzamide
N-METHOXY-N-METHYLBENZAMIDE
Benzamide, N-methoxy-N-methyl-
Methyl N-methylbenzohydroxamate
N-Methoxy-N-methylbenzamide >
N-Methoxy-N-methylbenzenecarboxamide
N-Benzoyl-N-methyl-O-methylhydroxylamine
N-Methylbenzohydroxamic acid methyl ester
[Molecular Formula]

C9H11NO2
[MDL Number]

MFCD00075320
[MOL File]

6919-61-5.mol
[Molecular Weight]

165.19
Chemical PropertiesBack Directory
[Boiling point ]

70 °C0.1 mm Hg(lit.)
[density ]

1.085 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.533(lit.)
[Fp ]

>230 °F
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Liquid
[color ]

Colorless to yellow
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

2928009090
Hazard InformationBack Directory
[Uses]

N-Methoxy-N-methylbenzamide may be used in the preparation of β-trifluoromethyl enaminones.
[Uses]

N-Methoxy-N-methylbenzamide is used to prepare orally bioavailable tetrasubstituted imidazoles as inhibitors of p38 mitogen-activated protein kinase. It is used to synthesize benzofuran and benzothiophene biphenyls as inhibitors of protein tyrosine phosphatase 1B with antihyperglycemic properties.
[Definition]

ChEBI: The Weinreb amide of benzoic acid.
[General Description]

N-Methoxy-N-methylbenzamide is an N,N-disubstituted benzamide. also referred as Weinreb amide., Hydrogen bonding interactions between thioacetamide and N-methoxy-N-methylbenzamide has been investigated using near-infrared absorption spectroscopy. Preparation of N-methoxy-N-methylbenzamide has been reported.
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