67735-51-7

Basic information

• Product Name: N-methyl-N-phenylfuran-2-carboxamide
• Synonyms: 2-furancarboxamide, N-methyl-N-phenyl-; N-Methyl-N-phenyl-2-furamide
• CAS NO: 67735-51-7
• Molecular Formula: C₁₂H₁₁NO₂
• Molecular Weight: 201.2212
• Mol File: 67735-51-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 318.5°C at 760 mmHg
• Flash Point: 146.4°C
• Density: 1.186g/cm³
• Vapor Pressure: 0.000361mmHg at 25°C
• Refractive Index: 1.597
• CAS DataBase Reference: N-methyl-N-phenylfuran-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-phenylfuran-2-carboxamide(67735-51-7)
• EPA Substance Registry System: N-methyl-N-phenylfuran-2-carboxamide(67735-51-7)

Safety Data

• Hazardous Substances Data: 67735-51-7(Hazardous Substances Data)

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 100-61-8 N-methylaniline 
• 98-01-1 furfural 
• 121-69-7 N,N-dimethyl-aniline 
• 611-13-2 2-furoic acid methyl ester 
• 63633-79-4 N-(furan-2-carbonyl) saccharin 

Downstream Products

• 20895-16-3 1-(2-Furanyl)-3-methyl-1-butanone 
• 17572-16-6 furan-2-carbothioic acid-(N-methyl-anilide) 
• 1982-62-3 N-(p-tolyl)furan-2-carboxamide 

Relevant articles and documents

Nickel-Catalyzed Oxidative Transamidation of Tertiary Aromatic Amines with N -Acylsaccharins

The use of tertiary amines as surrogates for secondary amines has prominent advantages in terms of stabilization and ease of handling. A Ni-catalyzed transamidation of N -acylsaccharins with tertiary aromatic amines is reported. By using tert -butyl hydroperoxide as the terminal oxidant, this reaction permits selective cleavage of the C(sp 3)-N bonds of unsymmetrical tertiary aromatic amines depending on the sizes of the alkyl substituents.

Alternating current electrolysis for organic electrosynthesis: Trifluoromethylation of (hetero)arenes

Paired electrolysis has a limited reaction scope for organic synthesis because it is often not compatible with reactions involving short-lived intermediates. We addressed this limitation using alternating current electrolysis (ACE). Using trifluoromethyla

Facile amidation of esters with aromatic amines promoted by lanthanide tris (amide) complexes

The development of catalysts capable of catalyzing amidation of esters with amines to construct amides under mild conditions is of great importance. Compared to aliphatic amines, the direct catalytic amidation of esters with less nucleophilic aromatic amines is rather difficult. Employing simple lanthanide tris (amide) complexes Ln[N (SiMe3)2]3(μ-Cl)Li (THF)3 as the catalysts, it was found a broad range of aromatic amines and esters were efficiently converted into various amides in good yields under mild conditions. A plausible mechanism for this transformation was experimentally supported as starting from an amide exchange reaction between the lanthanide tris (amide) complex and the substrate amine.