95482-82-9

Basic information

• Product Name: (E)-(R)-1-((R)-Toluene-4-sulfinyl)-pent-3-en-2-ol
• Synonyms: (E)-(R)-1-((R)-Toluene-4-sulfinyl)-pent-3-en-2-ol
• CAS NO: 95482-82-9
• Molecular Weight: 224.324
• Mol File: 95482-82-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-(R)-1-((R)-Toluene-4-sulfinyl)-pent-3-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-(R)-1-((R)-Toluene-4-sulfinyl)-pent-3-en-2-ol(95482-82-9)
• EPA Substance Registry System: (E)-(R)-1-((R)-Toluene-4-sulfinyl)-pent-3-en-2-ol(95482-82-9)

Safety Data

• Hazardous Substances Data: 95482-82-9(Hazardous Substances Data)

Upstream product

• 107866-63-7 (E)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-one 
• 95482-77-2 (R)-(E)-1-p-tolylsulfinyl-3-penten-2-one 

Downstream Products

• 107866-69-3 (R)-1-(Toluene-4-sulfonyl)-pentane-2,3,4-triol 
• 107866-69-3 (R)-1-(Toluene-4-sulfonyl)-pentane-2,3,4-triol 
• 116885-52-0 (E)-(R)-1-(Toluene-4-sulfonyl)-pent-3-en-2-ol 
• 116885-50-8 p-tolylsulfonyl 2-methoxy 3-pentene 
• 1569-50-2 (2S,3E)-pent-3-en-2-ol 

Relevant articles and documents

Stereospecific hydroxylation of chiral allylic β-hydroxysulfoxides: asymmetric synthesis of L-arabinitol

Chiral allylic β-hydroxysulfoxides 2 have been hydroxylated by the osmium tetroxide catalyzed reaction.The reaction can be highly stereoselective depending on the nature of the substituent linked to the double bond and the configurations of the sulfoxide and hydroxylic groups.The diastereoselectivity can be as high as 90 percent.This methodology was applied to the asymmetric synthesis of L-arabinitol.

Reduction of β-Keto Sulfoxides: A Highly Efficient Asymmetric Synthesis of Both Enantiomers of Allylic Alcohols

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