Name: 2-Methyl-1,5-hexadiene (97%)
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- Overview
  - 2-Methyl-1,5-hexadiene on mercury-photosensitized irradiation, undergoes internal cycloaddition to afford 1-methylbicyclo[2. 1. 1]hexane (as major product). High-temperature pyrolysis of 2-methyl-1,5-hexadiene affords 1,5-hexadiene and 2,5-dimethyl-1,5-hexadiene. 2-Methyl-1,5-hexadiene undergoes stereoselective and regioselective reaction with dialkylaluminum chloride (Et2AlCl) and titanium alkoxide [Ti(OPr-i)4, a catalyst] followed by oxidation to afford the corresponding five-membered 3-alkylcycloalkyl methanol. 2-Methyl-1,5-hexadiene is formed as a major product during the condensation reaction between allyl chloride and methallyl chloride in the presence of magnesium.
    
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- Properties
  - Categories
    
    Organic Building Blocks
    
    Alternative Name
    
    2-Methyldiallyl
    
    CAS Number
    
    4049-81-4
    
    Molecular Formula
    
    CH2=CHCH2CH2C(CH3)=CH2
    
    Molecular Weight
    
    96.17
    
    Purity
    
    97%
    
    SMILES
    
    CC(=C)CCC=C
    
    InChi
    
    1S/C7H12/c1-4-5-6-7(2)3/h4H,1-2,5-6H2,3H3
    
    InChi Key
    
    SLQMKNPIYMOEGB-UHFFFAOYSA-N
    
    MDL Number
    
    MFCD00008603
    
    Others
    
    SID 24879664
    
    Hazard Information
    
    Danger
    Flammable liquids
    
    Note
    
    Please note that Amerigo Scientific does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.
    
    * For Research Use Only.

2-Methyl-1,5-hexadiene (97%)

2-Methyl-1,5-hexadiene (97%)

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