51608-62-9

Basic information

• Product Name: Benzamide, N-(phenylmethylene)-, (E)-
• CAS NO: 51608-62-9
• Molecular Formula: C14H11NO
• Molecular Weight: 209.247
• Mol File: 51608-62-9.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(phenylmethylene)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(phenylmethylene)-, (E)-(51608-62-9)
• EPA Substance Registry System: Benzamide, N-(phenylmethylene)-, (E)-(51608-62-9)

Safety Data

• Hazardous Substances Data: 51608-62-9(Hazardous Substances Data)

Upstream product

• 120419-97-8 (E)-N-benzylidene-1,1,1-trimethylsilanamine 
• 98-88-4 benzoyl chloride 
• 100-52-7 benzaldehyde 
• 117067-48-8 1-benzotriazolyl-N-benzoyl-1-phenylmethylamine 
• 55-21-0 benzamide 
• 1816-89-3 2-azido-1-(1,2-diphenyl)ethanone 
• 17599-61-0 N-benzylidene-1,1,1-trimethylsilanamine 
• 10387-93-6 N-(methoxy(phenyl)methyl)benzamide 

Downstream Products

• 128407-14-7 2-<(benzoylamino)(phenyl)methyl>-4-methyl-3-morpholinone 
• 263239-91-4 (R)-3-((4R,6S)-2,4-Diphenyl-5,6-dihydro-4H-[1,3]oxazin-6-yloxy)-4,4-dimethyl-dihydro-furan-2-one 
• 263239-93-6 (R)-3-((4R,6R)-2,4-Diphenyl-5,6-dihydro-4H-[1,3]oxazin-6-yloxy)-4,4-dimethyl-dihydro-furan-2-one 
• 1000681-04-8 (R)-N-(1-phenylbut-3-en-1-yl)benzamide 
• 1000681-08-2 N-((1R,2R)-2-methyl-1-phenylbut-3-enyl)benzamide 

Relevant articles and documents

The highly enantioselective addition of indoles to N-acyl imines with use of a chiral phosphoric acid catalyst

Equation Presented The highly enantioselective organocatalytic addition of N-benzyl indoles to N-acyl imines is reported. A total of 15 examples with product yield ranging from 89% to 99% and enantioselectivities from 90% to 97% are presented. A chiral ph

High substrate/catalyst organocatalysis by a chiral Bronsted acid for an enantioselective aza-ene-type reaction

(Chemical Equation Presented) Lowering the load: A very small amount of a binaphthol-derived monophosphoric acid organocatalyst accelerates an azaene-type reaction of N-benzoylimines with enecarbamates to provide β-aminoimines with high enantiomeric purit

N-propargylamides via the asymmetric Michael addition of B-alkynyl-10-TMS-9-borabicyclo[3.3.2]decanes to N-acylimines

The asymmetric synthesis of N-propargylamides through Michael addition of the alkynylborane 1 to N-acylimines is reported. The N-acetylimines provide the best substrates for the process exhibiting high selectivity (56-95% ee) with predictable stereochemis