65755-66-0

Basic information

• Product Name: 5-Hexen-2-one, 3-(phenylthio)-
• CAS NO: 65755-66-0
• Molecular Formula: C12H14OS
• Molecular Weight: 206.309
• Mol File: 65755-66-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-Hexen-2-one, 3-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Hexen-2-one, 3-(phenylthio)-(65755-66-0)
• EPA Substance Registry System: 5-Hexen-2-one, 3-(phenylthio)-(65755-66-0)

Safety Data

• Hazardous Substances Data: 65755-66-0(Hazardous Substances Data)

Upstream product

• 882-33-7 diphenyldisulfane 
• 68843-70-9 pent-4-en-2-one (Z)-oxime 
• 69753-43-1 1-chloro-1-phenylthio-2-propanone 
• 762-72-1 allyl-trimethyl-silane 
• 5042-53-5 1-(phenylsulfanyl)acetone 
• 106-95-6 allyl bromide 
• 104260-84-6 3-Phenylsulfanyl-hex-5-en-2-one oxime 

Downstream Products

• 77119-57-4 3-acetyl-2-methyl-3-phenylthio-5-hexenal 
• 551-45-1 allethrolone 
• 77119-59-6 3-allyl-4-methyl-5-nitro-3-phenylthio-2-pentanone 

Relevant articles and documents

Stereoselective synthesis of (±)-urechitol A employing [4+3] cycloaddition

Urechitol A was synthesized as a racemate employing a [4+3] cycloaddition reaction and a methanol assisted intramolecular epoxide opening as key steps for efficient construction of the core tricyclic framework. The overall yield was 2.4% over 12 steps.

CHEMOSELECTIVE REACTION OF ALLYLSILANES WITH α-CHLOROSULFIDES CONTAINING A CARBONYL GROUP

Allylsilanes (2) reacted with α-chlorosulfides (1) containing a carbonyl group either at α, β, or γ position to substitute exclusively for the chlorine atom of 1, and the corresponding α-allylsulfides (3) were obtained in high yields.

Convenient Method for Regiospecific Carbon-Carbon Bond Formation at the γ Position of Allylic Halides

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