CAS 6270-17-3
:Benzenebutanoic acid, γ-oxo-, ethyl ester
Description:
Benzenebutanoic acid, γ-oxo-, ethyl ester, with the CAS number 6270-17-3, is an organic compound characterized by its ester functional group and a benzene ring. This compound features a butanoic acid backbone with a ketone (γ-oxo) group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical reactions and processes. Typically, compounds of this nature exhibit moderate to low toxicity, but safety precautions should always be taken when handling them. The structure allows for potential interactions with biological systems, which may lead to applications in pharmaceuticals or agrochemicals. Additionally, the compound may participate in various chemical reactions, such as esterification or condensation, making it a versatile intermediate in synthetic organic chemistry. Overall, benzenebutanoic acid, γ-oxo-, ethyl ester is a valuable compound in both industrial and research settings due to its unique structural features and reactivity.
Formula:C12H14O3
InChI:InChI=1S/C12H14O3/c1-2-15-12(14)9-8-11(13)10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
InChI key:InChIKey=BRUOEHVDTAORQY-UHFFFAOYSA-N
SMILES:C(CCC(OCC)=O)(=O)C1=CC=CC=C1
Synonyms:- 3-Carbethoxy-1-phenyl-1-propanone
- 4-Phenyl-4-oxobutanoic acid ethyl ester
- Ai3-07012
- Benzenebutanoic acid, gamma-oxo-, ethyl ester
- Benzenebutanoic acid, γ-oxo-, ethyl ester
- Ethyl 3-benzoylpropionate
- Ethyl 4-Oxo-4-Phenylbutanoate
- Ethyl 4-phenyl-4-oxobutanoate
- Ethyl γ-oxobenzenebutanoate
- NSC 10083
- NSC 33812
- Propionic acid, 3-benzoyl-, ethyl ester
- Ethyl 4-oxo-4-phenylbutyrate
- See more synonyms
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Found 4 products.
Benzenebutanoic acid, g-oxo-, ethyl ester
CAS:Formula:C12H14O3Purity:98%Color and Shape:LiquidMolecular weight:206.2378Ethyl 4-Oxo-4-phenylbutanoate
CAS:Ethyl 4-Oxo-4-phenylbutanoatePurity:95%Molecular weight:206.24g/molEthyl 4-oxo-4-phenylbutyrate
CAS:<p>Ethyl 4-oxo-4-phenylbutyrate is a butyrophenone that is used as an intermediate in organic synthesis. It is produced by the reaction of ethyl diazoacetate with peroxide, followed by the addition of propiophenone and regiospecific solvents. This reaction can be carried out using organocatalysts or without them. The optimised conditions for this type of reaction are: a temperature of 20 °C, an alkylation time of 1 hour, and a molecular weight range from 200 to 600 g/mol. Ethyl 4-oxo-4-phenylbutyrate has been shown to react with carbenes and stereospecific solvents in order to produce levulinate.</p>Formula:C12H14O3Purity:Min. 95%Molecular weight:206.24 g/mol




