79996-62-6

Basic information

• Product Name: 4,6-Heptadien-3-ol, (E)-
• CAS NO: 79996-62-6
• Molecular Formula: C7H12O
• Molecular Weight: 112.172
• Mol File: 79996-62-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,6-Heptadien-3-ol, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-Heptadien-3-ol, (E)-(79996-62-6)
• EPA Substance Registry System: 4,6-Heptadien-3-ol, (E)-(79996-62-6)

Safety Data

• Hazardous Substances Data: 79996-62-6(Hazardous Substances Data)

Upstream product

• 88920-63-2 1-((1S,3R,7R)-4,4-Dioxo-4λ⁶-thia-tricyclo[5.2.1.0^2,6]dec-8-en-3-yl)-propan-1-ol 

Downstream Products

• 73321-47-8 methyl <<<(1-ethyl-2,4-pentadienyl)oxy>carbonyl>amino><<(phenylamino)carbonyl>oxy>acetate 
• 73321-50-3 (5R,8aR)-1-Ethyl-3-oxo-hexahydro-oxazolo[3,4-a]pyridine-5-carboxylic acid 
• 79996-65-9 (5R,8aR)-1-Ethyl-3-oxo-hexahydro-oxazolo[3,4-a]pyridine-5-carboxylic acid 4-nitro-benzyl ester 
• 30915-43-6 E,Z-heptatriene 
• 17679-93-5 (3E,5E)-1,3,5-heptatriene 

Relevant articles and documents

Une synthese hautement stereoselective de dienes conjugues (E)

A general method for the preparation of (E) terminal conjugated dienes was developed by the flash thermolysis of 2-substituted 2,5-dihydrothiophene-1,1-dioxides generated by a retro Diels-Alder reaction.This process allows the obtention of conjugated dienes, bearing or not a functionality (alcohols, esters), with an excellent stereoisomeric purity (in general higher than 98percent).An application to the synthesis of (E)-9,11-dodecadien-1-yl acetate, the major component of the sex pheromone of Diparopsis castanea, shows the generality and the efficacy of this method.