162131-80-8

Basic information

• Product Name: (R)-5,6-epoxy-1-(4-methoxybenzyl)oxy-2-hexyne
• Synonyms: (R)-5,6-epoxy-1-(4-methoxybenzyl)oxy-2-hexyne
• CAS NO: 162131-80-8
• Molecular Weight: 232.279
• Mol File: 162131-80-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-5,6-epoxy-1-(4-methoxybenzyl)oxy-2-hexyne(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-5,6-epoxy-1-(4-methoxybenzyl)oxy-2-hexyne(162131-80-8)
• EPA Substance Registry System: (R)-5,6-epoxy-1-(4-methoxybenzyl)oxy-2-hexyne(162131-80-8)

Safety Data

• Hazardous Substances Data: 162131-80-8(Hazardous Substances Data)

Upstream product

• 51594-55-9 (R)-(-)-epichlorohydrin 
• 4039-83-2 3-(4-methoxybenzyloxy)propyne 

Downstream Products

• 81506-24-3 [3S-(1Z,3α,5β)]-2-[3,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methylenecyclohexylidene]ethanol 
• 162131-83-1 (S)-5-(t-butyldimethylsilyl)oxy-9-(4-methoxybenzyl)oxy-2,7-nonadiyn-1-ol 
• 162131-84-2 (S,E)-5-(t-butyldimethylsilyl)oxy-9-(4-methoxybenzyl)oxynona-2-en-7-yn-1-ol 
• 162131-86-4 (3S,5R)-5-(t-butyldimethylsilyl)oxy-9-(4-methoxybenzyl)oxynona-1-en-7-yn-3-ol 
• 162131-85-3 (2S,3S,5R)-2,3-epoxy-5-(t-butyldimethylsilyl)oxy-9-(4-methoxybenzyl)oxy-7-nonyn-1-ol 
• 162131-79-5 tert-Butyl-[(R)-1-((2S,3R)-3-iodomethyl-oxiranylmethyl)-5-(4-methoxy-benzyloxy)-pent-3-ynyloxy]-dimethyl-silane 
• 162131-87-5 (3S,5R)-3,5-di(t-butyldimethylsilyl)oxy-9-(4-methoxybenzyl)oxynona-1-en-7-yne 
• 162131-90-0 Methanesulfonic acid (2S,3S)-3-[(R)-2-(tert-butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hex-4-ynyl]-oxiranylmethyl ester 
• 162131-82-0 (R)-5-(t-butyldimethylsilyl)oxy-9-(t-butyldiphenylsilyl)oxy-1-(4-methoxybenzyl)oxy-2,7-nonadiyne 
• 162131-81-9 (R)-9-(t-butyldiphenylsilyl)oxy-1-(4-methoxybenzyl)oxy-2,7-nonadiyn-5-ol 

Relevant articles and documents

An efficient route to a key A-ring synthon for 1α,25-dihydroxyvitamin D3 and its analogs

An efficient and highly stereoselective route to the Roche's A-ring synthon of 1α,25-dihydroxyvitamin D3 from R-(-)-epichlorohydrin has been developed utilizing double propargylation of R-(-)-epichlorohydrin and palladium(0) catalyzed intramole