1275581-35-5

Basic information

• Product Name: (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate
• Synonyms: (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate
• CAS NO: 1275581-35-5
• Molecular Weight: 304.386
• Mol File: 1275581-35-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate(1275581-35-5)
• EPA Substance Registry System: (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate(1275581-35-5)

Safety Data

• Hazardous Substances Data: 1275581-35-5(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 112790-78-0 (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol 

Downstream Products

• 1275581-38-8 diethyl 2-((3'S,4'R)-4'-(benzyloxy)hexa-1',5'-dien-3'-yl)malonate 
• 1275581-42-4 (2S,3S,4R)-methyl 4-(benzyloxy)-2-(prop-2-ynyl)-3-vinylhex-5-enoate 
• 1275581-43-5 (2R,3S,4R)-methyl 4-(benzyloxy)-2-(prop-2-ynyl)-3-vinylhex-5-enoate 
• 1275581-41-3 (3R,4R)-methyl-4-(benzyloxy)-3-vinylhex-5-enoate 

Relevant articles and documents

Desymmetrization of (R,R)-hexa-1,5-diene-3,4-diol via monofunctionalization and rhodium-catalyzed allylic substitution

A sequence of selective monoprotection and Rh-catalyzed enantioconservative allylic substitution is established as a desymmetrization strategy for C 2-symmetric hexa-1,5-diene-3,4-diol. A benzyl protecting group and ethyl carbonate as a leaving