159730-67-3

Basic information

• Product Name: benzyl 4-formylbenzylcarbamate
• Synonyms: benzyl 4-formylbenzylcarbamate
• CAS NO: 159730-67-3
• Molecular Formula: C₁₆H₁₅NO₃
• Molecular Weight: 269.3
• Mol File: 159730-67-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 68 °C
• Boiling Point: 478.1±38.0 °C(Predicted)
• Appearance: /
• Density: 1.205±0.06 g/cm3(Predicted)
• PKA: 11.71±0.46(Predicted)
• CAS DataBase Reference: benzyl 4-formylbenzylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 4-formylbenzylcarbamate(159730-67-3)
• EPA Substance Registry System: benzyl 4-formylbenzylcarbamate(159730-67-3)

Safety Data

• Hazardous Substances Data: 159730-67-3(Hazardous Substances Data)

Upstream product

• 63914-51-2 [(4-cyanophenyl)methyl]-carbamic acid phenylmethyl ester 
• 1075221-26-9 benzyl [4-(1,3-dioxolan-2-yl)benzyl]carbamate 
• 501-53-1 benzyl chloroformate 
• 39895-56-2 4-hydroxymethyl-benzylamine 
• 1020415-08-0 (4-((((benzyloxy)carbonyl)amino)methyl)phenyl)methanol 

Downstream Products

• 1075221-28-1 C₂₄H₂₄N₂O₃ 
• 1608150-71-5 tert-butyl ((S)-1-(((3S,6S,7R,9aS)-3-(benzhydrylcarbamoyl)-7-(2-((4-((((benzyloxy)carbonyl)amino)methyl)benzyl)(tert-butoxycarbonyl)amino)ethyl)-5-oxooctahydro-1H-pyrrolo[1,2-a]azepin-6-yl)amino)-1-oxobutan-2-yl)(methyl)carbamate 
• 1608150-72-6 tert-butyl ((S)-1-(((3S,6S,7R,9aS)-3-(benzhydrylcarbamoyl)-7-(2-((4-((((benzyloxy)carbonyl)amino)methyl)benzyl)(tert-butoxycarbonyl)amino)ethyl)-5-oxooctahydro-1H-pyrrolo[1,2-a]azepin-6-yl)amino)-1-oxobutan-2-yl)(methyl)carbamate 
• 1608150-73-7 4-((4-(((2-((3S,6S,7R,9aS)-3-(benzhydrylcarbamoyl)-6-((S)-2-((tertbutoxycarbonyl)(methyl)amino)butanamido)-5-oxooctahydro-1H-pyrrolo[1,2-a]azepin-7-yl)ethyl)(tert-butoxycarbonyl)amino)methyl)benzyl)amino)-4-oxobutanoic acid 
• 1608150-70-4 tert-butyl ((S)-1-(((3S,6S,7R,9aS)-3-(benzhydrylcarbamoyl)-7-(2-((4-((((benzyloxy)carbonyl)amino)methyl)benzyl)amino)ethyl)-5-oxooctahydro-1H-pyrrolo[1,2-a]azepin-6-yl)amino)-1-oxobutan-2-yl)(methyl)carbamate 

Relevant articles and documents

Photoswitchable sensitization of porphyrin excited states

Light-driven molecular switches consisting of a porphyrin covalently linked to a fulgimide photochrome antenna have been prepared. Light absorbed by the cyclic form of the fulgimide is transferred to the porphyrin with ? 95% efficiency, generating the por

Synthesis of α,α-difluoro-β-amino esters or gem-difluoro-β-lactams as potential metallocarboxypeptidase inhibitors

The synthesis of gem-difluorinated β-lactams and gem-difluorinated β-amino acids, each possessing a potential basic functional group, from ethyl bromodifluoroacetate and either imines (for β-lactams) or N-(α-aminoalkyl)benzotriazoles (for β-amino esters) was investigated. A series of these compounds were used for the design of novel metallocarboxypeptidase inhibitors. N-Alkylation and N-acylation of these two versatile scaffolds were carried out, leading to the expected targets in moderate to good yields. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.