61495-08-7

Basic information

• Product Name: N-(4-methoxy-2-methylphenyl)benzamide
• CAS NO: 61495-08-7
• Molecular Formula: C₁₅H₁₅NO₂
• Molecular Weight: 241.2851
• Mol File: 61495-08-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 305.3°C at 760 mmHg
• Flash Point: 138.4°C
• Density: 1.156g/cm³
• Vapor Pressure: 0.000831mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: N-(4-methoxy-2-methylphenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxy-2-methylphenyl)benzamide(61495-08-7)
• EPA Substance Registry System: N-(4-methoxy-2-methylphenyl)benzamide(61495-08-7)

Safety Data

• Hazardous Substances Data: 61495-08-7(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 102-50-1 2-methyl-4-methoxyaniline 
• 2581-34-2 3-methyl-4-nitrophenol 
• 5367-32-8 5-methoxy-2-nitrotoluene 

Downstream Products

• 147779-39-3 2-benzoylamino-5-methoxy-benzoic acid 
• 5883-96-5 5-methoxy-2-phenylindole 
• 375385-70-9 N-(4,4-dimethoxy-2-methyl-cyclohexa-2,5-dienylidene)-benzamide 
• 375385-76-5 [8-(benzoylamino)-5-methoxy-7-methyl-1,4-dihydronaphthalen-1-yl]methyl pivalate 
• 1214752-42-7 N,N'-bis(2-methyl-4-methoxyphenyl)-N-benzoylbenzamidine 
• 1616268-50-8 4-([1,4'-bipiperidin]-1'-ylmethyl)-1-methyl-2-phenyl-1H-indol-5-ol 
• 117616-09-8 5-methoxy-1-methyl-2-phenyl-1H-indole 
• 101096-87-1 5-hydroxy-1-methyl-2-phenyl-1H-indole 

Relevant articles and documents

Chiral Br?nsted Acid from Chiral Phosphoric Acid Boron Complex and Water: Asymmetric Reduction of Indoles

A new chiral Br?nsted acid, generated in situ from a chiral phosphoric acid boron (CPAB) complex and water, was successfully applied to asymmetric indole reduction. This “designer acid catalyst”, which is more acidic than TsOH as suggested by DFT calculations, allows the unprecedented direct asymmetric reduction of C2-aryl-substituted N-unprotected indoles and features good to excellent enantioselectivities with broad functional group tolerance. DFT calculations and mechanistic experiments indicates that this reaction undergoes C3-protonation and hydride-transfer processes. Besides, bulky C2-alkyl-substituted N-unprotected indoles are also suitable for this system.

Anxiolytic-like effects of N,N-dialkyl-2-phenylindol-3-ylglyoxylamides by modulation of translocator protein promoting neurosteroid biosynthesis

Novel N,N-disubstituted indol-3-ylglyoxylamides (1-56), bearing different combinations of substituents R1-R5, were synthesized and evaluated as ligands of the translocator protein (TSPO), the 18 kDa protein representing the minimal f

2-Substituted indoles and process for their preparation

Highly branched α-substituted indoles, e.g., 2-(1-methylcyclohexyl)-indole, are prepared by treating N-(α-branched carbonyl) toluidines with alkyl lithium. The reaction sequence may be illustrated as SPC1