139125-56-7

Basic information

• Product Name: Cyclohexanone, 2-methyl-2-(2-oxopropyl)-, (R)-
• CAS NO: 139125-56-7
• Molecular Formula: C10H16O2
• Molecular Weight: 168.236
• Mol File: 139125-56-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-methyl-2-(2-oxopropyl)-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-methyl-2-(2-oxopropyl)-, (R)-(139125-56-7)
• EPA Substance Registry System: Cyclohexanone, 2-methyl-2-(2-oxopropyl)-, (R)-(139125-56-7)

Safety Data

• Hazardous Substances Data: 139125-56-7(Hazardous Substances Data)

Upstream product

• 139125-46-5 (3S,6R,7aR)-6-But-3-enyl-3-isopropyl-6,7a-dimethyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one 
• 139125-50-1 (3S,6R,7aR)-6-(4-Hydroxy-butyl)-3-isopropyl-6,7a-dimethyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one 
• 98203-44-2 (3S,7aR)-3-isopropyl-7a-methyltetrahydropyrrolo[2,1-b][1,3]-oxazol-5-one 
• 917-64-6 methyl magnesium iodide 
• 139125-52-3 (3S,6R,7aR)-6-(4-Bromo-butyl)-3-isopropyl-6,7a-dimethyl-tetrahydro-pyrrolo[2,1-b]oxazol-5-one 

Downstream Products

• 54725-16-5 8-Methyl-Δ³-hydrinden-2-on 

Relevant articles and documents

Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)CI: Access to enantiomerically enriched all-carbon quaternary centers

The catalytic asymmetric α-alkylation of tributyltin enolates with a range of primary alkyl halides is catalyzed by a chiral Cr(salen) complex. The reaction constitutes the first transition-metal-catalyzed system for α-alkylation of carbonyl substrates wi