215026-14-5

Basic information

• Product Name: (1S,2S,1'S)-2-(cyclohex-2'-enyloxy)-1,2-diphenylethanol
• Synonyms: (1S,2S,1'S)-2-(cyclohex-2'-enyloxy)-1,2-diphenylethanol
• CAS NO: 215026-14-5
• Molecular Weight: 294.393
• Mol File: 215026-14-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,1'S)-2-(cyclohex-2'-enyloxy)-1,2-diphenylethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,1'S)-2-(cyclohex-2'-enyloxy)-1,2-diphenylethanol(215026-14-5)
• EPA Substance Registry System: (1S,2S,1'S)-2-(cyclohex-2'-enyloxy)-1,2-diphenylethanol(215026-14-5)

Safety Data

• Hazardous Substances Data: 215026-14-5(Hazardous Substances Data)

Upstream product

• 2325-10-2 (S,S)-hydrobenzoin 

Downstream Products

• 215026-15-6 (1S,3S,4S,6S,7S)-3,4-diphenyl-7-phenylseleno-2,5-dioxabicyclo[4,4,0]decane 
• 215026-28-1 (1S,3S,4S,6S,7S,8R,9R)-3,4-diphenyl-2,5-dioxa-7-tert-butyldiphenylsilyloxy-8,9-epoxybicyclo[4,4,0]decane 
• 215026-22-5 (1S,3S,4S,6S,7S,8S)-3,4-diphenyl-2,5-dioxa-7,8-epoxybicyclo[4,4,0]decane 
• 849596-45-8 (1S,3S,4S,6S,7S,8S,9S)-3,4-diphenyl-2,5-dioxa-7-tert-butyldiphenylsilyloxy-9-phenylselenobicyclo[4,4,0]decan-8-ol 
• 849596-47-0 (1S,3S,4S,6S,7S,8R)-3,4-diphenyl-2,5-dioxa-7-tert-butyldiphenylsilyloxybicyclo[4,4,0]dec-9-en-8-ol 
• 215026-27-0 (1S,3S,4S,6S,7S)-3,4-diphenyl-2,5-dioxa-7-tert-butyldiphenylsilyloxybicyclo[4,4,0]dec-8-ene 
• 215026-34-9 (1S,3S,4S,6R,7S,8R,9R,10R)-3,4-diphenyl-2,5-dioxabicyclo-[4,4,0]decane-7,8,9,10-tetrol 
• 215026-25-8 (1S,3S,4S,6R,7S,8R,9R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]decane-7,8,9-triol 
• 849596-43-6 (1S,3S,4S,6R,7S,8S)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]decane-7,8-diol 
• 215026-33-8 (1S,3S,4S,6R,7S,8R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-9-ene-7,8-diol 
• 215026-24-7 (1S,3S,4S,6R,7S)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-8-en-7-ol 
• 849596-42-5 (1S,3S,4S,6R)-3,4-diphenyl-2,5-dioxabicyclo[4,4,0]dec-7-ene 
• 849596-44-7 [1S-(1α,2α,3β,4β)]-cyclohexane-1,2,3,4-tetrol 
• 81369-59-7 3-deoxy-epi-inositol 

Relevant articles and documents

Transformation of cyclohexene to enantiopure cyclitols mediated by sequential oxyselenenylation with (S,S)-hydrobenzoin: Synthesis of D-chiro-inositol and muco-quercitol

Oxyselenenylation of cyclohexene with (S,S)-hydrobenzoin and subsequent oxidation-elimination allows isolation of an allylic ether in which further phenylselenenylation is completely regioselective, thus allowing entry to the cyclitols D-chiro-inositol and muco-quercitol.