4127-43-9

Basic information

• Product Name: (1R,2R,4R)-4-tert-butyl-1-phenylcyclohexane-1,2-diol
• Synonyms: 1,2-Cyclohexanediol, 4-(1,1-dimethylethyl)-1-phenyl-, (1alpha,2alpha,4alpha)-
• CAS NO: 4127-43-9
• Molecular Formula: C₁₆H₂₄O₂
• Molecular Weight: 248.3606
• Mol File: 4127-43-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 360.2°C at 760 mmHg
• Flash Point: 162.6°C
• Density: 1.083g/cm³
• Vapor Pressure: 8.13E-06mmHg at 25°C
• Refractive Index: 1.553
• CAS DataBase Reference: (1R,2R,4R)-4-tert-butyl-1-phenylcyclohexane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R,4R)-4-tert-butyl-1-phenylcyclohexane-1,2-diol(4127-43-9)
• EPA Substance Registry System: (1R,2R,4R)-4-tert-butyl-1-phenylcyclohexane-1,2-diol(4127-43-9)

Safety Data

• Hazardous Substances Data: 4127-43-9(Hazardous Substances Data)

Upstream product

• 3419-73-6 1-phenyl-4-tert-butylcyclohexene 

Relevant articles and documents

An investigative study of kinetic resolutions by the Sharpless asymmetric dihydroxylation reaction

The requirements for a highly selective kinetic resolution with the Sharpless asymmetric dihydroxylation (AD) reaction were investigated with a number of alkene substrates. It was found that with 1-phenyl-4-tert-butylcyclohexene enantioselectivity is very high, yet diastereoselectivity is poor and kinetic resolution is ineffective. With 5-methyl-2-phenylbicyclo[3.2.0]heptan-2-ene both diastereoselectivity and enantioselectivity are high and kinetic resolution is effective. It was discovered that the transition state for the product-determining step in the Sharpless AD reaction is not product-like, and effective kinetic resolution can occur when one face of a chiral alkene is hindered.