273381-23-0

Basic information

• Product Name: (3aS,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-one
• Synonyms: (3aS,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-one
• CAS NO: 273381-23-0
• Molecular Weight: 290.359
• Mol File: 273381-23-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3aS,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-one(273381-23-0)
• EPA Substance Registry System: (3aS,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-one(273381-23-0)

Safety Data

• Hazardous Substances Data: 273381-23-0(Hazardous Substances Data)

Upstream product

• 273381-21-8 tert-Butyl-[(3aS,4S,6R,6aS)-2,2-dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-yloxy]-dimethyl-silane 
• 273381-20-7 (1R,2S,3S,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-5-(1-methyl-1-phenyl-ethoxy)-cyclopentane-1,2-diol 
• 258834-31-0 tert-Butyl-dimethyl-[(1S,4R)-4-(1-methyl-1-phenyl-ethoxy)-cyclopent-2-enyloxy]-silane 
• 258834-27-4 (-)-cis-1-acetoxy-4-cumyloxy-2-cyclopentene 
• 258834-30-9 (-)-cis-4-Cumyloxy-2-cyclopenten-1-ol 
• 57702-56-4 cis- and trans-4-cumyloxy-2-cyclopentenol 
• 65457-77-4 4-<(1,1'-dimethylbenzyl)oxy>-2-cyclopentenone 
• 273381-22-9 (3aR,4S,6R,6aS)-2,2-Dimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-ol 

Downstream Products

• 104010-72-2 (3aS,6aS)-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-one 
• 273381-24-1 (3aS,4R,6R,6aS)-2,2,4-Trimethyl-6-(1-methyl-1-phenyl-ethoxy)-tetrahydro-cyclopenta[1,3]dioxol-4-ol 

Relevant articles and documents

An enantiodivergent route to α-cuparenone utilizing chiral cyclopentenol having a latent meso structure

An efficient enantiodivergent route to α-cuparenone, a sesquiterpene isolated in both enantiomeric forms, has been developed utilizing a chiral cyclopentanoid starting material having a latent meso structure. (C) 2000 Elsevier Science Ltd.