CAS 495-41-0
:1-Phenyl-2-buten-1-one
Description:
1-Phenyl-2-buten-1-one, also known as phenylbutenone, is an organic compound characterized by its conjugated double bond system and a ketone functional group. It features a phenyl group attached to a butenone structure, which contributes to its reactivity and potential applications in organic synthesis. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the double bond and the carbonyl group makes it susceptible to various chemical reactions, including nucleophilic addition and electrophilic substitution. 1-Phenyl-2-buten-1-one is often used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as it may pose health risks if inhaled or ingested.
Formula:C10H10O
InChI:InChI=1S/C10H10O/c1-2-6-10(11)9-7-4-3-5-8-9/h2-8H,1H3
InChI key:InChIKey=FUJZJBCWPIOHHN-UHFFFAOYSA-N
SMILES:C(C=CC)(=O)C1=CC=CC=C1
Synonyms:- (2E)-1-phenylbut-2-en-1-one
- 1-Benzoylpropene
- 1-Phenyl-But-2-En-1-One
- 1-Phenylbut-2-En-1-One
- 1-Propenyl phenyl ketone
- 2-Buten-1-one, 1-phenyl-
- 2-Butenophenone
- Crotonophenone
- Ethylideneacetophenone
- Nsc 518668
- Phenyl 1-propenyl ketone
- Phenyl propenyl ketone
- See more synonyms
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Found 5 products.
1-Phenyl-2-buten-1-one
CAS:<p>1-Phenyl-2-buten-1-one</p>Purity:80%Color and Shape:LiquidMolecular weight:146.19g/molPhenyl 1-Propenyl Ketone
CAS:Formula:C10H10OPurity:>80.0%(GC)Color and Shape:White to Yellow to Green clear liquidMolecular weight:146.191-Phenyl-2-buten-1-one
CAS:<p>1-Phenyl-2-buten-1-one is a ketone that is produced by the Friedel-Crafts reaction, which entails the use of an aluminum chloride catalyst in the presence of hydroxy groups. This chemical can also be produced by a reductive carbonylation reaction using acetaldehyde and an organic solvent. <br>This chemical has been shown to have reductase activities and coordination geometry. It has also been shown to inhibit enzyme activities such as β-unsaturated ketones reductase, indole alkaloid reductase, and acetaldehyde dehydrogenase. The optimal reaction for this compound is borohydride reduction. 1-Phenyl-2-buten-1-one has not been isolated in yields greater than 90%.</p>Formula:C10H10OPurity:Min. 95%Molecular weight:146.19 g/mol




