98017-34-6

Basic information

• Product Name: Cycloheptanone, 2-hydroxy-2-phenyl-
• CAS NO: 98017-34-6
• Molecular Formula: C13H16O2
• Molecular Weight: 204.269
• Mol File: 98017-34-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cycloheptanone, 2-hydroxy-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cycloheptanone, 2-hydroxy-2-phenyl-(98017-34-6)
• EPA Substance Registry System: Cycloheptanone, 2-hydroxy-2-phenyl-(98017-34-6)

Safety Data

• Hazardous Substances Data: 98017-34-6(Hazardous Substances Data)

Upstream product

• 3008-39-7 cycloheptane-1,2-dione 
• 14996-78-2 2-phenylcycloheptanone 
• 7472-43-7 6-benzoylhexanoic acid 
• 870262-29-6 1-imidazol-1-yl-7-phenyl-heptane-1,7-dione 

Downstream Products

• 855405-77-5 2-phenyl-cyclohept-2-enone-(2,4-dinitro-phenylhydrazone) 
• 65825-75-4 2-phenylcyclohept-2-en-1-one 

Relevant articles and documents

Bronsted Acid Mediated Direct α-Hydroxylation of Cyclic α-Branched Ketones

We report a Bronsted acid mediated direct α-hydroxylation of cyclic α-branched ketones via a tandem aminoxylation/N-O bond-cleavage process. Nitrosobenzene is used as the oxidant and subsequently promotes the liberation of the free alcohol. The desired pr

Electroreductive acylation of aromatic ketones with acylimidazoles

The intermolecular reductive coupling of aromatic ketones with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-trimethylsiloxy ketones and esters. The best result was obtained using Bu4NPF6 as a supporting electrolyte and a Pb cathode in THF. The α-trimethylsiloxy-containing products were transformed to the corresponding α-hydroxy ketones and esters by treatment with TBAF in THF. This method was also effective for the intramolecular reductive coupling of δ- and ε-keto acylimidazoles.