
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:C8H14OPurity:>96.0%(GC)Color and Shape:Colorless to Yellow to Green clear liquidMolecular weight:126.203-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:C8H14OPurity:97%Color and Shape:Colorless to pale yellow, LiquidMolecular weight:126.203-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 formFormula:C8H14OPurity:Min. 95%Molecular weight:126.2 g/mol