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CAS 1669-44-9: 3-Octen-2-one

Formula:C8H14O
InChI:InChI=1S/C8H14O/c1-3-4-5-6-7-8(2)9/h6-7H,3-5H2,1-2H3
InChI key:InChIKey=ZCFOBLITZWHNNC-UHFFFAOYSA-N
SMILES:C(=CC(C)=O)CCCC
Synonyms:
  • (3E)-oct-3-en-2-one
  • (E)-Oct-3-en-2-one
  • 1-Hexenyl methyl ketone
  • 3-Octen-2-one, (E)-
  • Fema 3416
  • Oct-3-En-2-One
  • Trans-2,4-Undecadienal
  • Trans-3-Octen-2-One
  • 3-Octen-2-one
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Found 6 products.
  • 3-Octen-2-one

    CAS:
    Formula:C8H14O
    Purity:>96.0%(GC)
    Color and Shape:Colorless to Yellow to Green clear liquid
    Molecular weight:126.20

    Ref: 3B-O0252

    5ml
    27.00€
    25ml
    72.00€
  • 3-Octen-2-one, 97%

    CAS:
    This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
    Formula:C8H14O
    Purity:97%
    Color and Shape:Colorless to pale yellow, Liquid
    Molecular weight:126.20

    Ref: 02-A14652

    10g
    To inquire
    50g
    To inquire
    250g
    To inquire
  • 3-Octen-2-One

    CAS:
    3-Octen-2-One
    Purity:97%
    Molecular weight:126.2g/mol

    Ref: 54-OR1028894

    1g
    32.00€
    5g
    36.00€
    25g
    117.00€
    100g
    368.00€
    500g
    1,506.00€
  • 3-Octen-2-one

    CAS:
    Formula:C8H14O
    Color and Shape:Neat

    Ref: TR-O456005

    1g
    75.00€
  • 3-Octen-2-one

    CAS:
    Formula:C8H14O
    Purity:97%
    Color and Shape:Liquid
    Molecular weight:126.1962

    Ref: IN-DA001X02

    1g
    30.00€
    5g
    63.00€
    25g
    142.00€
  • 3-Octen-2-one

    CAS:
    3-Octen-2-one is an organic compound that belongs to the class of ketones. It is a colorless liquid with a strong odor. 3-Octen-2-one has been shown to be a possible precursor in the synthesis of the natural product astragali radix, which has been found to have antiinflammatory, antispasmodic, and antiviral properties. The most common route for the synthesis of 3-octen-2-one is by acid catalyzed dehydration of octanal. This reaction takes place in two steps: first, octanal reacts with hydrochloric acid to produce 2-octanol; second, this intermediate reacts with water to form 3-octen-2-one. A number of other reactions are also possible for this chemical including esterification and oxidation reactions. The carbonyl group in 3-octen-2-one can react with an alcohol or amine group from another molecule to form
    Formula:C8H14O
    Purity:Min. 95%
    Molecular weight:126.2 g/mol

    Ref: 3D-BAA66944

    250g
    Discontinued
    Discontinued product