| Identification | Back 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 Properties | Back 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 |
| Hazard Information | Back 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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