94966-17-3

Basic information

• Product Name: naphthalene-1-carboxylic acid naphthalen-1-yl ester
• Synonyms: naphthalene-1-carboxylic acid naphthalen-1-yl ester
• CAS NO: 94966-17-3
• Molecular Weight: 298.341
• Mol File: 94966-17-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: naphthalene-1-carboxylic acid naphthalen-1-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: naphthalene-1-carboxylic acid naphthalen-1-yl ester(94966-17-3)
• EPA Substance Registry System: naphthalene-1-carboxylic acid naphthalen-1-yl ester(94966-17-3)

Safety Data

• Hazardous Substances Data: 94966-17-3(Hazardous Substances Data)

Upstream product

• 29903-04-6 di(1-naphthoyl) peroxide 
• 90-15-3 α-naphthol 
• 879-18-5 naphthalene-1-carbonic acid chloride 

Downstream Products

• 432047-72-8 1-naphthalenyl-[4-(pentoxy)-1-naphthalenyl]methanone 

Relevant articles and documents

Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone: A potent, orally bioavailable human CB1/CB2 dual agonist with antihyperalgesic properties and restricted central nervous system penetration

Selective activation of peripheral cannabinoid CB1 receptors has the potential to become a valuable therapy for chronic pain conditions as long as central nervous system effects are attenuated. A new class of cannabinoid ligands was rationally

Behavior of naphthoyloxyl and methoxynaphthoyloxyl radicals generated from the photocleavage of dinaphthoyl peroxides and 1-(naphthoyloxy)-2-pyridones

1-Naphthoyloxyl and 2-naphthoyloxyl radicals were generated from photocleavage of dinaphthoyl peroxides and 1-(naphthoyloxy)-2-pyridones in acetonitrile. The difference in product distribution between the precursors is ascribed to the contribution of the two-bond cleavage in the peroxide decomposition in the singlet state. A series of methoxynaphthoyloxyl radicals were also generated from the corresponding (methoxynaphthoyloxy)pyridones and their behavior was compared with that of unsubstituted naphthoyloxyl radicals. The introduction of a methoxy group in the naphthalene ring stabilizes the naphthoyloxyl radicals to prevent their decarboxylation completely and reduces remarkably their reactivities in the addition to olefins and hydrogen-atom abstraction. The structure of the naphthoyloxyl radicals was discussed on the basis of their absorption spectra and MO calculations.