1021245-67-9

Basic information

• Product Name: 2-[(4-methoxyphenyl)amino]-N-methylacetamide
• Synonyms: 2-[(4-methoxyphenyl)amino]-N-methylacetamide
• CAS NO: 1021245-67-9
• Molecular Weight: 194.233
• Mol File: 1021245-67-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-[(4-methoxyphenyl)amino]-N-methylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-methoxyphenyl)amino]-N-methylacetamide(1021245-67-9)
• EPA Substance Registry System: 2-[(4-methoxyphenyl)amino]-N-methylacetamide(1021245-67-9)

Safety Data

• Hazardous Substances Data: 1021245-67-9(Hazardous Substances Data)

Upstream product

• 34680-81-4 2-bromo-N-methylacetamide 
• 104-94-9 4-methoxy-aniline 
• 598-21-0 2-Bromoacetyl bromide 
• 74-89-5 methylamine 

Downstream Products

• 1073534-48-1 C₁₈H₁₇BrN₂O₂ 
• 1073534-47-0 C₂₄H₂₂N₂O₂ 
• 1073534-51-6 C₁₉H₂₀N₂O₃ 
• 1073534-42-5 C₁₈H₁₈N₂O₂ 
• 1073534-49-2 C₁₉H₂₀N₂O₂ 
• 345-32-4 5-(trifluoromethyl)isatin 
• 1370469-90-1 6-methoxy-N-methyl-4-phenylquinoline-2-carboxamide 
• 1205585-34-7 C₁₀H₁₂N₂O₂ 
• 1370469-93-4 4-(4-chlorophenyl)-6-methoxy-N-methylquinoline-2-carboxamide 
• 1370469-92-3 4-(4-(tert-butyl)phenyl)-6-methoxy-N-methylquinoline-2-carboxamide 

Relevant articles and documents

Enantioselective synthesis of arylglycine derivatives by direct C-H oxidative cross-coupling

A new method for the synthesis of chiral α-amino acid derivatives by enantioselective C-H arylation of N-aryl glycine esters with aryl boric acids in the presence of a chiral Pd(ii)-catalyst has been developed. This work successfully integrates the direct C-H oxidation with asymmetric arylation and exhibits excellent enantioselectivity. This journal is

Copper Triflate Catalyzed Oxidative α-Allylation of Glycine Derivatives

Copper triflate catalyzed oxidative C-H functionalization of glycine derivatives with allyltributyltin has been established using oxygen or tert -butyl hydroperoxide as oxidant. Various glycine esters and glycine amides were suitable substrates for this oxidative allylation reaction and afforded the desired homoallylic amines in moderate to good yields.

Functionalizing glycine derivatives by direct C-C bond formation

(Chemical Equation Presented) Come on glycine: Two different types of glycine derivatives are α-functionalized using cross-dehydrogenative- coupling (CDC) reactions. The method allows the efficient attachment of a malonate or aromatic alkyne group on the α-position of the glycine derivatives under very mild conditions.