117286-14-3

Basic information

• Product Name: (2R,3S)-1,2-epoxy-3-(tosyloxy)tetradecane
• Synonyms: (2R,3S)-1,2-epoxy-3-(tosyloxy)tetradecane
• CAS NO: 117286-14-3
• Molecular Weight: 382.565
• Mol File: 117286-14-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2R,3S)-1,2-epoxy-3-(tosyloxy)tetradecane(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-1,2-epoxy-3-(tosyloxy)tetradecane(117286-14-3)
• EPA Substance Registry System: (2R,3S)-1,2-epoxy-3-(tosyloxy)tetradecane(117286-14-3)

Safety Data

• Hazardous Substances Data: 117286-14-3(Hazardous Substances Data)

Upstream product

• 117316-14-0 erythro-(2R,3S)-1-(Tosyloxy)-2,3-tetradecanediol 
• 92318-78-0 (2R,3R,S)-1,2,3-Tetradecanetriol 
• 128898-79-3 (2S,3S)-2,3-Epoxy-1-tetradecanol 
• 211310-85-9 (S)-tetradec-1-en-3-ol 
• 17642-48-7 (+/-)-1-Tetradecen-3-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 150822-82-5 erythro-(2R,3S)-1,2-Epoxy-3-tetradecanol 
• 112-54-9 Dodecanal 
• 138093-67-1 (+/-)-1,2-Epoxy-3-tetradecanol 

Downstream Products

• 117286-18-7 threo-10-tosyloxy-3,6-heneicosadiyn-9-ol 
• 117286-18-7 (+/-)-threo-10-(Tosyloxy)-3,6-heneicosadiyn-9-ol 
• 233279-62-4 (9S,10S)-9-hydroxy-10-(tosyloxy)henicosa-3,6-diyne 
• 162758-32-9 (9S,10S)-9-hydroxy-10-tosyloxyheneicosadec-6-yne 
• 98230-44-5 (Z)-(+/-)-cis-2-(2-Octynyl)-3-undecyloxirane 
• 98230-44-5 cis-(+/-)-(Z)-2-(2-octenyl)-3-undecyloxirane 

Relevant articles and documents

Concise total synthesis of (3Z,6Z,9S,10R)-9,10-epoxy-1,3,6-heneicosatriene, sex pheromone component of Hyphantria Cunea

The total synthesis of (3Z,6Z,9S,10R)-9,10-epoxy-1,3,6-heneicosatriene, sex pheromone component of Hyphantria cunea, using a convergent synthetic strategy, was achieved through the regioselective coupling of the two fragments, chiral epoxy tosylate and 1,

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