19340-86-4

Basic information

• Product Name: N-benzyl-4-(benzyloxy)butanamide
• Synonyms: N-benzyl-4-(benzyloxy)butanamide
• CAS NO: 19340-86-4
• Molecular Weight: 283.37
• Mol File: 19340-86-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-4-(benzyloxy)butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-4-(benzyloxy)butanamide(19340-86-4)
• EPA Substance Registry System: N-benzyl-4-(benzyloxy)butanamide(19340-86-4)

Safety Data

• Hazardous Substances Data: 19340-86-4(Hazardous Substances Data)

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 10385-30-5 4-(benzyloxy)butanoic acid 
• 100-46-9 benzylamine 
• 4541-14-4 4-benzyloxy-butan-1-ol 
• 20194-18-7 sodium phenyl-methanolate 

Downstream Products

• 19340-87-5 N-<γ-Benzyloxy-butyryl>-phenylessigsaeure-benzylamid 
• 19340-89-7 γ-Phenylacetoxy-buttersaeure-benzylamid 
• 7500-45-0 N-benzylphenylacetamide 
• 118602-97-4 ethyl 4-[(phenylmethyl)oxy]butanoate 
• 19340-88-6 N-benzyl-4-hydroxybutanamide 

Relevant articles and documents

Compounds with cardiac myosin activating function and pharmaceutical composition containing the same for treating or preventing heart failure

The present invention relates to a compound having a cardiotonic activating function and a pharmaceutical composition containing the same. The composition comprising the compound according to the present invention is effective in preventing or treating heart failure. In addition, the compound is represented by chemical formula 2 or is pharmaceutically acceptable salt thereof.COPYRIGHT KIPO 2016

Selective catalytic sp3 C-O bond cleavage with C-N bond formation in 3-alkoxy-1-propanols

The ruthenium catalyzed selective sp3 C-O cleavage with amide formation was reported in reactions of 3-alkoxy-1-propanol derivatives and amines. The cleavage only occurs at the C3-O position even with 3-benzyloxy-1-propanol. Based on the experimental results, O-bound and C-bound Ru enolate complexes were proposed as key intermediates for the unique selective sp3 C-O bond cleavage in 3-alkoxy-1-propanols.