795279-40-2

Basic information

• Product Name: (2R,3R)-2-(5-methoxycyclohexa-1,4-dienyl)-4-methylpentan-2-ol
• CAS NO: 795279-40-2
• Molecular Weight: 210.316
• Mol File: 795279-40-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R)-2-(5-methoxycyclohexa-1,4-dienyl)-4-methylpentan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-2-(5-methoxycyclohexa-1,4-dienyl)-4-methylpentan-2-ol(795279-40-2)
• EPA Substance Registry System: (2R,3R)-2-(5-methoxycyclohexa-1,4-dienyl)-4-methylpentan-2-ol(795279-40-2)

Safety Data

• Hazardous Substances Data: 795279-40-2(Hazardous Substances Data)

Upstream product

• 795279-39-9 (2S,3R)-2-(3-methoxyphenyl)-4-methylpentan-3-ol 

Downstream Products

• 147659-07-2 (+)-prelactone B 
• 224580-59-0 (3S,4S,5R)-3-Hydroxy-4,6-dimethylheptanoic acid δ-lactone 

Relevant articles and documents

Application of sulfur ylide mediated epoxidations in the asymmetric synthesis of β-hydroxy-δ-lactones. Synthesis of a mevinic acid analogue and (+)-prelactone B

Catalytic and stoichiometric asymmetric sulfur ylide reactions were employed to prepare alkyl-aryl epoxide intermediates in a convergent manner. These epoxides were utilized in efficient syntheses of the mevinic acid analogue 1 and prelactone B. Graphical abstract.