119137-01-8

Basic information

• Product Name: Anthracen-2-yl-carbamic acid 4,5-dimethoxy-2-nitro-benzyl ester
• Synonyms: Anthracen-2-yl-carbamic acid 4,5-dimethoxy-2-nitro-benzyl ester
• CAS NO: 119137-01-8
• Molecular Weight: 432.433
• Mol File: 119137-01-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Anthracen-2-yl-carbamic acid 4,5-dimethoxy-2-nitro-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracen-2-yl-carbamic acid 4,5-dimethoxy-2-nitro-benzyl ester(119137-01-8)
• EPA Substance Registry System: Anthracen-2-yl-carbamic acid 4,5-dimethoxy-2-nitro-benzyl ester(119137-01-8)

Safety Data

• Hazardous Substances Data: 119137-01-8(Hazardous Substances Data)

Upstream product

• 1016-58-6 6-nitroveratryl alcohol 
• 17017-03-7 2-anthraceneisocyanate 
• 613-13-8 2-aminoanthracene 
• 42855-00-5 nitroveratryloxycarbonyl chloride 

Downstream Products

• 613-13-8 2-aminoanthracene 
• 119137-07-4 4,5-dimethoxy-2-nitrosobenzaldehyde 

Relevant articles and documents

PHOTOACTIVABLE FLUOROPHORES. 1. SYNTHESIS AND PHOTOACTIVATION OF o-NITROBENZYL-QUENCHED FLUORESCENT CARBAMATES

The synthesis and photoactivation of a new type of fluorescent probe, the photoactivable fluorophore (PAF) are described.The PAFs described in this paper consist of fluorescent aromatic amines coupled to substituted nitrobenzyl quenching chromophores via a carbamate linkage.Photoactivation occurs by an intramolecular photo-redox reaction, converting the o-nitrosobenzaldehyde hemiacetal which fragments with loss of CO2 to liberate the fluorescent amine.Photoactivation quantum yields also are reported.