68487-09-2

Basic information

• Product Name: 2-Pentanone, 1-hydroxy-1-phenyl-
• CAS NO: 68487-09-2
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 68487-09-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Pentanone, 1-hydroxy-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pentanone, 1-hydroxy-1-phenyl-(68487-09-2)
• EPA Substance Registry System: 2-Pentanone, 1-hydroxy-1-phenyl-(68487-09-2)

Safety Data

• Hazardous Substances Data: 68487-09-2(Hazardous Substances Data)

Upstream product

• 93-89-0 benzoic acid ethyl ester 
• 105-54-4 butanoic acid ethyl ester 
• 20895-66-3 1-phenyl-1,2-pentanedione 
• 1569272-11-2 phenyl(2-propyl-1,3-dithian-2-yl)methanol 
• 100-52-7 benzaldehyde 
• 123-72-8 butyraldehyde 
• 31675-43-1 diethyl 1-phenyl-1-(trimethylsiloxy)methanephosphonate 
• 21663-35-4 1-phenyl-pent-3-ene-1,2-diol 
• 50265-96-8 N-tert-butyl-N'-butylidenehydrazine 
• 71292-80-3 diethyl 1-trimethylsilyloxy-2-oxo-1-phenylpentylphosphonate 
• 10557-57-0 propylmagnesium iodide 
• 774-40-3 hydroxy-phenyl-acetic acid ethyl ester 
• 532-28-5 (RS)-mandelonitrile 
• 4410-31-5 (RS)-mandelamide 

Relevant articles and documents

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

Polymer-supported synthesis of α- and β-hydroxyketones through the formation of 1,3-dithiane intermediates

The synthesis of polymer-supported 2-monosubstituted 1,3-dithianes from soluble copolymers bearing 1,3-propanedithiol groups, their lithiation, reactions with electrophiles such as aldehydes, ketones, α,β- unsaturated ketones and oxiranes, and cleavage of

AZO ANIONS IN SYNTHESIS. PT 1. t-BUTYLHYDRAZONES AS ACYL-ANION EQUIVALENTS

The lithium salts of aldehyde t-butylhydrazones react with electrophiles (aldehydes, ketones, alkyl halides, crotonates) to form C-trapped t-butylazo-compounds; tautomerisation and hydrolysis gave α-hydroxy ketones, ketones, and γ-keto esters in good yield, thereby providing a convenient new acyl-anion equivalent.Reaction of these lithium salts with aldehydes and ketones, followed by elimination provided a new route to azo alkenes.