112790-78-0

Basic information

• Product Name: (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol
• Synonyms: (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol
• CAS NO: 112790-78-0
• Molecular Weight: 204.269
• Mol File: 112790-78-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol(112790-78-0)
• EPA Substance Registry System: (3R,4R)-4-benzyloxy-hexa-1,5-dien-3-ol(112790-78-0)

Safety Data

• Hazardous Substances Data: 112790-78-0(Hazardous Substances Data)

Upstream product

• 1069-23-4 (3R,4R)-1,5-hexadiene-3,4-diol 
• 100-39-0 benzyl bromide 
• 112699-61-3 C₂₄H₃₀O₁₆S₄ 
• 112723-62-3 Acetic acid (1S,2S,3R)-2-benzyloxy-1-((R)-1,2-bis-methanesulfonyloxy-ethyl)-3,4-bis-methanesulfonyloxy-butyl ester 
• 7462-38-6 O³,O⁴-dibenzoyl-D-mannitol 
• 130282-82-5 D_g-threo-dibenzoyloxy-hexadiene-(1.5) 
• 69-65-8 mannitol 

Downstream Products

• 1027731-14-1 (R)-5-((E)-(R)-1-Benzyloxy-tridec-2-enyl)-5H-furan-2-one 
• 1275581-33-3 (3R,4R)-4-(benzyloxy)-hexa-1,5-dien-3-yl methyl carbonate 
• 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 
• 1275581-38-8 diethyl 2-((3'S,4'R)-4'-(benzyloxy)hexa-1',5'-dien-3'-yl)malonate 
• 1275581-34-4 (3R,4R)-4-(benzyloxy)-hexa-1,5-dien-3-yl ethyl carbonate 
• 1275581-35-5 (3R,4R)-4-(benzyloxy)hexa-1,5-dien-3-yl tert-butyl carbonate 
• 1200-22-2 (R)-1,2-dithiolane-3-pentanoic acid 
• 112699-67-9 (E)-(R)-6-Benzyloxy-8-hydroxy-oct-4-enoic acid ethyl ester 
• 866885-85-0 (5S)-3-[(R)-13-hydroxy-13-((R)-5-oxotetrahydrofuran-2-yl)tridecyl]-5-methyl-3-(phenylsulfanyl)dihydrofuran-2-one 
• 102339-68-4 1,2-Anhydro-4-O-benzyl-5,6-didesoxy-D-lyxo-hex-5-enitol 
• 1005759-10-3 (3R,4R)-3-benzyloxy-4-allyloxyhexa-1,5-diene 
• 928307-05-5 (2S,3R,4R)-1,2-epoxy-4-(benzyloxy)-hex-5-en-3-ol 

Relevant articles and documents

Bidirectional Synthesis of 6-Acetoxy-5-hexadecanolide, the Mosquito Oviposition Pheromone of Culex quinquefasciatus, from a C2-Symmetric Building Block Using Olefin Metathesis Reactions

(5R,6S)-6-Acetoxy-5-hexadecanolide (MOP) is the oviposition pheromone of the mosquito Cx. quinquefasciatus, a vector of pathogens causing a variety of tropical diseases. We describe and evaluate herein three syntheses of MOP starting from mannitol-derived

Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis

(Chemical Equation Presented) A strategy for the synthesis of chiral 5-(1-hydroxyalk-2-enyl)-5H-furan-2-ones and its application to the total synthesis of (-)-muricatacin, in four steps and 37% overall yield from (R,R)-hexa-1,5-diene-3,4-diol, are describ