94339-72-7

Basic information

• Product Name: (2R,3R,4R,6S)-7-Benzyloxymethoxy-2,4,6-trimethyl-heptane-1,3-diol
• CAS NO: 94339-72-7
• Molecular Weight: 310.434
• Mol File: 94339-72-7.mol

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R,6S)-7-Benzyloxymethoxy-2,4,6-trimethyl-heptane-1,3-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,6S)-7-Benzyloxymethoxy-2,4,6-trimethyl-heptane-1,3-diol(94339-72-7)
• EPA Substance Registry System: (2R,3R,4R,6S)-7-Benzyloxymethoxy-2,4,6-trimethyl-heptane-1,3-diol(94339-72-7)

Safety Data

• Hazardous Substances Data: 94339-72-7(Hazardous Substances Data)

Upstream product

• 94339-71-6 [(2S,3R)-3-((1R,3S)-4-Benzyloxymethoxy-1,3-dimethyl-butyl)-2-methyl-oxiranyl]-methanol 

Downstream Products

• 79495-87-7 protomycinolide IV 
• 94339-73-8 Acetic acid (1S,2S,4R)-1-((S)-2-acetoxy-1-methyl-ethyl)-5-benzyloxymethoxy-2,4-dimethyl-pentyl ester 

Relevant articles and documents

TOTAL SYNTHESIS OF PROTOMYCINOLIDE IV

A 16-membered macrolide antibiotic, protomycinolide IV, was synthesized from two fragments to which the chirality was introduced by asymmetric epoxidation of the appropriately chosen allylic alcohols.A new synthesis of the Prelog-Djerassi lactonic acid from one of the intermediates of the synthesis was also carried out.