112403-78-8

Basic information

• Product Name: Benzeneacetamide, N-methoxy-
• CAS NO: 112403-78-8
• Molecular Formula: C9H11NO2
• Molecular Weight: 165.192
• Mol File: 112403-78-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzeneacetamide, N-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetamide, N-methoxy-(112403-78-8)
• EPA Substance Registry System: Benzeneacetamide, N-methoxy-(112403-78-8)

Safety Data

• Hazardous Substances Data: 112403-78-8(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 593-56-6 N-methoxylamine hydrochloride 
• 67-62-9 O-Methylhydroxylamin 
• 738-75-0 (S)-3-phenyl-2-phenylacetylamino-propionic acid 
• 14773-47-8 2-phenyl-N-(3-phenylpropyl)acetamide 
• 112404-03-2 potassium phenylacetohydroxamate 
• 74-88-4 methyl iodide 
• 103-80-0 phenylacetyl chloride 

Downstream Products

• 101-97-3 Ethyl 2-phenylethanoate 
• 103-82-2 phenylacetic acid 
• 593-56-6 N-methoxylamine hydrochloride 
• 14773-47-8 2-phenyl-N-(3-phenylpropyl)acetamide 
• 1402345-74-7 N-methoxy-2-phenyl-N-pyridin-3-ylacetamide 
• 1402345-59-8 N-methoxy-N-(4-nitrophenyl)-2-phenylacetamide 
• 121990-00-9 N-methoxy-N-phenyl-2-phenylacetamide 
• 1402345-61-2 N-methoxy-N-(3-nitrophenyl)-2-phenylacetamide 
• 1402345-79-2 N-methoxy-N-(2-methylphenyl)-2-phenylacetamide 
• 1402345-72-5 N-(4-chlorophenyl)-N-methoxy-2-phenylacetamide 
• 1402345-62-3 N-(4-acetylphenyl)-N-methoxy-2-phenylacetamide 
• 1402345-66-7 N-methoxy-N-(3-methoxyphenyl)-2-phenylacetamide 
• 1402345-67-8 N-methoxy-2-phenyl-N-(4-tolyl)acetamide 
• 1402345-71-4 N-(4-bromophenyl)-N-methoxy-2-phenylacetamide 

Relevant articles and documents

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N-Aryl-O-alkylhydroxamic acid derivatives were prepared by copper-catalyzed cross-coupling of hydroxamates with aryl iodides. The reaction conditions are compatible with standard hydroxy-protecting groups on the hydroxylamine moiety and are applicable to

Three-component condensations of aldehydes with N-methoxycarboxamides

The first condensations of N-methoxycarboxamides (component A) with aliphatic acetals (component B) are described. Depending upon the conditions, the hemiaminal type products (AB) can usually be isolated. Conducting the condensations with 2 equiv of acetal affords β-(N-methoxy)amido aldehydes (type ABB products). A condensation using anisole (component C) afforded a product of type ABC.