176487-03-9

Basic information

• Product Name: (2S,3S)-4-cyclohexyl-2,3-epoxybutan-1-ol
• Synonyms: (2S,3S)-4-cyclohexyl-2,3-epoxybutan-1-ol
• CAS NO: 176487-03-9
• Molecular Weight: 170.252
• Mol File: 176487-03-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3S)-4-cyclohexyl-2,3-epoxybutan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-4-cyclohexyl-2,3-epoxybutan-1-ol(176487-03-9)
• EPA Substance Registry System: (2S,3S)-4-cyclohexyl-2,3-epoxybutan-1-ol(176487-03-9)

Safety Data

• Hazardous Substances Data: 176487-03-9(Hazardous Substances Data)

Upstream product

• 105198-42-3 ethyl (2E)-4-cyclohexyl-2-butenoate 
• 1589-44-2 (E)-4-cyclohexyl-2-buten-1-ol 

Downstream Products

• 176487-02-8 (2S,3R)-3-Bromo-4-cyclohexyl-2-hydroxy-butyric acid isopropyl ester 
• 176487-01-7 (2R,3S)-3-Cyclohexylmethyl-oxirane-2-carboxylic acid isopropyl ester 
• 176487-04-0 (2R,3S)-3-Cyclohexylmethyl-oxirane-2-carboxylic acid 

Relevant articles and documents

Prompt determination of absolute configuration for epoxy alcohols via exciton chirality protocol

A microscale protocol for determination of absolute configurations of 2,3-epoxy alcohols is described. 2,3-Disubstituted (cis and trans), 2,2-disubstituted, 2,2,3-trisubstituted, and 2,3,3-trisubstituted epoxy alcohols rendered prominent ECCD signals upon complexing with a Lewis acidic porphyrin tweezer and consequently provide straightforward assignment of chirality for epoxy alcohols. This method proved to be rapid, simple, sensitive, and reliable for the class of molecules listed above. Copyright

Stereoselective preparation of syn α-hydroxy-β-amino ester units via regioselective opening of α,β-epoxy esters: Enantioselective synthesis of taxol C-13 side chain and cyclohexylnorstatine

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