1361254-00-3

Basic information

• Product Name: (10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-8-ylmethyl)carbamic acid benzyl ester
• Synonyms: (10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-8-ylmethyl)carbamic acid benzyl ester
• CAS NO: 1361254-00-3
• Molecular Weight: 404.466
• Mol File: 1361254-00-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-8-ylmethyl)carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-8-ylmethyl)carbamic acid benzyl ester(1361254-00-3)
• EPA Substance Registry System: (10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-8-ylmethyl)carbamic acid benzyl ester(1361254-00-3)

Safety Data

• Hazardous Substances Data: 1361254-00-3(Hazardous Substances Data)

Upstream product

• 41175-50-2 8-hydroxyjulolidine 
• 82961-77-1 methyl 4-<(benzyloxycarbonyl)amino>-3-oxobutanoate 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 

Relevant articles and documents

A mild titanium-catalyzed synthesis of functionalized amino coumarins as fluorescence labels

In contrast to Bronsted and other Lewis acids ClTi(OiPr)3 is especially suited to catalyze the formation of amino-substituted coumarins from aminophenols and functionalized β-oxo esters in a Pechmann condensation. This straightforward protocol allows the synthesis of fluorescence labels and false fluorescent neurotransmitters.