1039357-66-8

Basic information

• Product Name: (3R,6S)-6-para-methoxybenzyloxyhept-1-en-3-ol
• Synonyms: (3R,6S)-6-para-methoxybenzyloxyhept-1-en-3-ol
• CAS NO: 1039357-66-8
• Molecular Weight: 250.338
• Mol File: 1039357-66-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3R,6S)-6-para-methoxybenzyloxyhept-1-en-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,6S)-6-para-methoxybenzyloxyhept-1-en-3-ol(1039357-66-8)
• EPA Substance Registry System: (3R,6S)-6-para-methoxybenzyloxyhept-1-en-3-ol(1039357-66-8)

Safety Data

• Hazardous Substances Data: 1039357-66-8(Hazardous Substances Data)

Upstream product

• 1039357-65-7 C₁₄H₂₀O₃ 
• 2181-42-2 trimethylsulphonium iodide 
• 58917-26-3 (S)-sulcatol 
• 4630-06-2 6-methylhept-5-en-2-ol 
• 108-05-4 vinyl acetate 
• 1262206-00-7 (4S)-4-para-methoxybenzyloxypentanal 
• 110-93-0 6-Methyl-hept-5-en-2-on 

Downstream Products

• 1039357-67-9 C₁₇H₂₆O₄ 

Relevant articles and documents

A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: Application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide e

The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols.