29556-17-0

Basic information

• Product Name: 1-Naphthalenecarboxamide, N-hydroxy-N-phenyl-
• CAS NO: 29556-17-0
• Molecular Formula: C17H13NO2
• Molecular Weight: 263.296
• Mol File: 29556-17-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenecarboxamide, N-hydroxy-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenecarboxamide, N-hydroxy-N-phenyl-(29556-17-0)
• EPA Substance Registry System: 1-Naphthalenecarboxamide, N-hydroxy-N-phenyl-(29556-17-0)

Safety Data

• Hazardous Substances Data: 29556-17-0(Hazardous Substances Data)

Usage

Common uses

Manufacturing of pharmaceuticals (intermediate in production of anti-inflammatory and analgesic drugs), precursor in synthesis of organic compounds

Known for

Inhibiting activity of certain enzymes, useful in development of new medications

Hazardous

Potentially hazardous substance, should be handled with care in a controlled environment.

Upstream product

• 98-95-3 nitrobenzene 
• 100-65-2 N-Phenylhydroxylamine 
• 879-18-5 naphthalene-1-carbonic acid chloride 

Downstream Products

• 183175-18-0 N-(1-naphthoyl)-N-phenyl-O-(4-benzoylbenzoyl)hydroxylamine 
• 86-55-5 1-naphthalenecarboxylic acid 
• 586-96-9 Nitrosobenzene 
• 87503-49-9 N-(1-naphthoyl)-O-(p-toluoyl)-N-phenylhydroxylamine 
• 194494-50-3 O-benzoyl-N-(1-naphthoyl)-N-phenylhydroxylamine 
• 87503-51-3 N,O-di(1-naphthoyl)-N-phenylhydroxylamine 

Relevant articles and documents

Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine

Most important property of compartmentalized liquids such as micelles is that they have an ability to concentrate guest molecules into relatively small effective volumes and then to promote the re-encounter of such molecules. This property also makes mice

The Photolysis of N,O-Diacyl-N-phenylhydroxylamines

The photochemical decomposition of the title compounds yielded the rearrangement products derived from 1,3- and 1,5-aroyloxyl migrations in addition to the fragmentation products typical of the aroyloxyl and amido radicals, while only 1,3-aroyloxyl migration was observed on thermolysis.The results of crossover experiments indicate an intramolecular rearrangement, probably involving homolysis of the N-O bond in the excited states.Triplet quenching studies demonstrate that the rearrangement and fragmentation proceed exclusively via the first excited singlet state.No formation of the rearrangement products on triplet sensitization was expl ained on the basis of the spin multiplicity effects on a radical-radical recombination process within a solvent cage.