1627848-04-7

Basic information

• Product Name: C₁₅H₂₁IO₂
• CAS NO: 1627848-04-7
• Molecular Weight: 360.235
• Mol File: 1627848-04-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₂₁IO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₂₁IO₂(1627848-04-7)
• EPA Substance Registry System: C₁₅H₂₁IO₂(1627848-04-7)

Safety Data

• Hazardous Substances Data: 1627848-04-7(Hazardous Substances Data)

Upstream product

• 671798-21-3 ethyl (2E)-8-(benzyloxy)oct-2-enoate 
• 71126-73-3 6-benzyloxyhexan-1-ol 
• 101492-91-5 6-benzyloxy-1-hexanal 
• 100-39-0 benzyl bromide 
• 629-11-8 1,6-hexanediol 

Downstream Products

• 1608148-71-5 (1E,3S)-8-(benzyloxy)-1-[(4R,5S)-2,2-dimethyl-5-octyl-1,3-dioxolan-4-yl]oct-1-en-3-ol 
• 1608148-72-6 ({(1E,3S)-8-(benzyloxy)-1-[(4R,5S)-2,2-dimethyl-5-octyl-1,3-dioxolan-4-yl]oct-1-en-3-yl}oxy)(tert-butyl)(dimethyl)silane 
• 158991-69-6 (3S)-8-(benzyloxy)oct-1-en-3-ol 

Relevant articles and documents

Stereoselective total synthesis of Oxylipins: (6S,7E,9R,10S)-6,9,10- trihydroxyoctadec-7-enoic acid and (6z,8r,9r,10s)-8,9,10-trihydroxyoctadec-6- enoic acid

The stereoselective total syntheses of oxylipins 1b and 1c are described starting from readily accessible natural sugars via the Grubbs cross-metathesis, Wittig olefination, and Zn-mediated reductive elimination as key steps. Copyright