119624-69-0

Basic information

• Product Name: (2R,3R)-4-cyclohexyl-2,3-epoxybutan-1-ol
• Synonyms: (2R,3R)-4-cyclohexyl-2,3-epoxybutan-1-ol
• CAS NO: 119624-69-0
• Molecular Weight: 170.252
• Mol File: 119624-69-0.mol

Chemical Properties

• CAS DataBase Reference: (2R,3R)-4-cyclohexyl-2,3-epoxybutan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-4-cyclohexyl-2,3-epoxybutan-1-ol(119624-69-0)
• EPA Substance Registry System: (2R,3R)-4-cyclohexyl-2,3-epoxybutan-1-ol(119624-69-0)

Safety Data

• Hazardous Substances Data: 119624-69-0(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 165683-80-7 (2S,3S)-3-(benzhydrylamino)-4-cyclohexyl-1,2-butanediol 
• 180891-91-2 (2R,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-[(p-nitrobenzoyl)oxy]butane 
• 1054810-89-7 (2R,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-(1-ethoxyethoxy)butane 
• 180891-92-3 (2R,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol 
• 1053738-27-4 ethyl (2R,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-(1-ethoxyethoxy)butanoate 
• 1053254-61-7 (2R,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-(1-ethoxyethoxy)butanoic acid 
• 1054638-88-8 (2R,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-(1-ethoxyethoxy)-1-butanol 
• 165683-84-1 (2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol 
• 104882-03-3 (2S,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-1,2-butanediol 
• 133485-22-0 *,S^*)>-β-<<(1,1-dimethylethoxy)carbonyl>amino>-α-hydroxycyclohexanebutanoic acid, ethyl ester 
• 178421-69-7 (2S,3S)-3-azido-4-cyclohexyl-1,2-butanediol 

Relevant articles and documents

A convenient, stereodivergent approach to the enantioselective synthesis of N-Boc-aminoalkyl epoxides

An efficient, stereodivergent and enantioselective synthesis of N-Boc-aminoalkyl epoxides has been developed. Starting from enantiomerically enriched anti N-diphenylmethyl-3-amino-1,2-diols, and after a change in the nitrogen protecting group, an intramol

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