35301-62-3

Basic information

• Product Name: Acetamide, N-methoxy-N-phenyl-
• CAS NO: 35301-62-3
• Molecular Formula: C9H11NO2
• Molecular Weight: 165.192
• Mol File: 35301-62-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetamide, N-methoxy-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-methoxy-N-phenyl-(35301-62-3)
• EPA Substance Registry System: Acetamide, N-methoxy-N-phenyl-(35301-62-3)

Safety Data

• Hazardous Substances Data: 35301-62-3(Hazardous Substances Data)

Upstream product

• 3376-33-8 O-methyl acetophenone oxime 
• 5806-90-6 N-methoxyacetamide 
• 71-43-2 benzene 
• 1795-83-1 N-Phenylacetohydroxamic acid 
• 186581-53-3 diazomethane 
• 134810-87-0 N-isopropylacetoxyacetanilide 
• 134810-86-9 N-Phenyl-N-propionyloxy-acetamide 
• 32954-65-7 N,O-diacetylphenylhydroxylamine 
• 54542-07-3 1-phenyl-propan-1-one-O-methyl-oxime 
• 134810-88-1 O-phenylethanoyl-N-phenyl-acetohydroxamic acid 

Downstream Products

• 1795-83-1 N-Phenylacetohydroxamic acid 
• 93-26-5 2-methoxyacetanilide 

Relevant articles and documents

Anionic hetero[3,3] and [3,5][ rearrangements of hydroxylamine derivatives accompanied with N-O bond cleavage

Aromatic and aliphatic N,O-divinylhydroxylamine systems generated in situ from hydroxylamine derivatives smoothly undergo [3,3] rearrangement. The base-catalyzed formation and rearrangement of enolates or dienolates of N-aryl-O-acylhydroxylamines, N,O-dia

An Electrophilic Aromatic Substitution by N-Methoxyamides via Hypervalen Iodine Intermediates

Treatment of N-methoxyamides with hypervalent iodine compounds generates electron deficient nitrogen species which react intra- or intermolecularly with an aromatic group to give N-aryl-N-methoxyamides in good yields.