| Weight | 98.145 g/mol | 
|---|---|
| Formula | C6H10O | 
| Hydrogen Acceptors | 1 | 
| Hydrogen Donors | 1 | 
| Aromatic Rings | 0 | 
| Rotatable Bonds | 2 | 
2,4-HEXADIEN-1-OL (111-28-4, 17102-64-6)
sorbyl alcohol, (E,E)-isomer · sorbyl alcohol
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 LabBot
      - Regioselectivity in the Diels-Alder reaction of 8,8-dimethylnaphthalene-1,4,5(8H)-trione with 2,4-hexadien-1-ol (Tetrahedron, 1999)
 - Methyl Homologues of Methyl Jasmonate and Methyl Dihydrojasmonate (Hedione) from Sorbyl Alcohol (Helvetica Chimica Acta, 2004)
 - The Diels-Alder Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride: A Novel Preparation for the Undergraduate Organic Chemistry Laboratory Course (Journal of Chemical Education, 1997)
 - Demonstration of a Runaway Exothermic Reaction: DielsAlder Reaction of (2E,4E)-2,4-Hexadien-1-ol and Maleic Anhydride (Journal of Chemical Education, 2011)
 - Methyl Homologues of Methyl Jasmonate and Methyl Dihydrojasmonate (Hedione) from Sorbyl Alcohol. (ChemInform, 2004)
 - ChemInform Abstract: Synthesis of Pheromones. Part 10. An Improved Synthesis of 2,4- Hexadien-1-ol. (ChemInform, 2010)
 - 
            
            Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - sorbyl alcohol, (E,E)-isomer
 - sorbyl alcohol
 - 
          SMILESCC=CC=CCO
 - 
          InChIKeyMEIRRNXMZYDVDW-UHFFFAOYSA-N
 
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Synthesis
                
                Reactant
                
                
                 + 
                
                1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide 
                
                (Nicolaou IBX dehydrogenation)
                
              
              
        
            
                
                acetaldehyde 
                
                
                 + 
                
                Reactant
                
                (Wittig)
                
              
              
        
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 2,4-HEXADIEN-1-OL 
                  