98230-44-5

Basic information

• Product Name: (Z)-(+/-)-cis-2-(2-Octynyl)-3-undecyloxirane
• CAS NO: 98230-44-5
• Molecular Weight: 308.548
• Mol File: 98230-44-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (Z)-(+/-)-cis-2-(2-Octynyl)-3-undecyloxirane(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-(+/-)-cis-2-(2-Octynyl)-3-undecyloxirane(98230-44-5)
• EPA Substance Registry System: (Z)-(+/-)-cis-2-(2-Octynyl)-3-undecyloxirane(98230-44-5)

Safety Data

• Hazardous Substances Data: 98230-44-5(Hazardous Substances Data)

Upstream product

• 75039-85-9 cis-tetradec-2-ene-1-ol 
• 117286-14-3 (+/-)-threo-1,2-Epoxy-3-(tosyloxy)tetradecane 
• 138093-67-1 (+/-)-1,2-Epoxy-3-tetradecanol 
• 17642-48-7 (+/-)-1-Tetradecen-3-ol 
• 112-54-9 Dodecanal 
• 98230-40-1 cis-9-heneicosen-6-yne 
• 98230-39-8 1-chloro-cis-2-tetradecene 
• 51309-22-9 tetradec-2-yn-1-ol 
• 693-67-4 bromoundecane 
• 98230-41-2 (+/-)-cis-2-(2-Octynyl)-3-undecyloxirane 
• 108034-02-2 (2R,3S,5Z)-cis-2,3-epoxy-5-undecen-1-ol 
• 107996-43-0 (5Z)-cis-2R,3S-epoxy-1-O-p-toluenesulfonyl-undecen-1-ol 
• 98230-42-3 trans-9-heneicosen-6-yne 
• 91899-45-5 1-chloro-trans-2-tetradecene 

Relevant articles and documents

Alkylative Epoxide Rearrangement. A Stereospecific Approach to Chiral Epoxide Pheromones

The alkylative rearrangement of 1,2-epoxy-3-alkanol tosylates is applied to the synthesis of chiral epoxide pheromones.Attack at the terminal carbon atom of epoxy tosylates by lithioacetylenes and cyclization of the intermediate tosyloxy alcohols produces

SYNTHESIS OF (6Z)-CIS-9S,10R-EPOXYHENEICOSENE, A COMPONENT OF THE RUBY TIGER MOTH PHEROMONE

A 10-step synthesis of the titled pheromone and analogues from an acyclic derivative of D-Xylose is described.