CAS 64920-29-2
:Ethyl α-oxobenzenebutanoate
Description:
Ethyl α-oxobenzenebutanoate, with the CAS number 64920-29-2, is an organic compound that belongs to the class of esters. It is characterized by the presence of an ethyl group, a ketone functional group (α-oxo), and a benzene ring, which contributes to its aromatic properties. This compound typically appears as a colorless to pale yellow liquid with a pleasant odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. Ethyl α-oxobenzenebutanoate is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the carbonyl group, making it susceptible to nucleophilic attack, which is a key feature in many chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C12H14O3
InChI:InChI=1S/C12H14O3/c1-2-15-12(14)11(13)9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
InChI key:InChIKey=STPXIOGYOLJXMZ-UHFFFAOYSA-N
SMILES:C(CC(C(OCC)=O)=O)C1=CC=CC=C1
Synonyms:- 2-Oxo-4-Phenyl Butanoic acid ethyl ester
- 2-Oxo-4-Phenylbutanoic Acid Ethyl Ester
- 2-Oxo-4-Phenylbutyric Acid Ethyl Ester
- 4-Phenyl-2-Oxobutyric Acid Ethyl Ester
- Benzenebutanoic acid, α-oxo-, ethyl ester
- Benzylpyruvic Acid Ethyl Ester
- Eopb
- Ethyl 2-Oxo-4-Phenylbutanoate
- Ethyl 3-benzylpyruvate
- Ethyl 4-phenyl-2-ketobutyrate
- Ethyl 4-phenyl-2-oxobutanoate
- Ethyl 4-phenyl-2-oxobutyrate
- Ethyl Benzylpyruvate
- Ethyl α-oxobenzenebutanoate
- Ethyl-2 Oxo-4 Phenyl Butanoate
- Keto Ester
- See more synonyms
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Found 8 products.
Ethyl 2-oxo-4-phenylbutyrate, 90+%
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 SciFormula:C12H14O3Purity:90+%Color and Shape:Liquid, Clear yellowMolecular weight:206.24Ethyl 2-Oxo-4-Phenylbutyrate
CAS:Ethyl 2-Oxo-4-PhenylbutyrateFormula:C12H14O3Purity:92%Molecular weight:206.24Ethyl 2-oxo-4-phenylbutanoate
CAS:Formula:C12H14O3Purity:92%Color and Shape:LiquidMolecular weight:206.2378Ethyl 2-oxo-4-phenylbutyrate (>90%)
CAS:Controlled ProductApplications Ethyl 2-oxo-4-phenylbutyrate (93%) (cas# 64920-29-2) is a compound useful in organic synthesis.
Formula:C12H14O3Purity:>90%Color and Shape:NeatMolecular weight:206.24Ethyl 2-oxo-4-phenylbutanoate
CAS:Formula:C12H14O3Purity:techColor and Shape:Liquid, ClearMolecular weight:206.241Ethyl 2-oxo-4-phenylbutanoate
CAS:Ethyl 2-oxo-4-phenylbutanoateFormula:C12H14O3Purity:92%Molecular weight:206.24Ethyl 2-oxo-4-phenylbutyrate
CAS:Ethyl 2-oxo-4-phenylbutyrate is a compound that belongs to the class of ester compounds. This molecule is found in cells grown in recombinant cultures and has been identified by its FTIR spectroscopy. Ethyl 2-oxo-4-phenylbutyrate inhibits the growth of candida glabrata by inhibiting an enzyme, which is involved in the conversion of glucose to acetoin. The mechanism for this inhibition is believed to be due to cinchonidine, which reacts with chloride ions. The chemical stability of ethyl 2-oxo-4-phenylbutyrate has been shown by its ability to withstand acidic pH and high concentrations of chloride ions without decomposing. Ethyl 2-oxo-4-phenylbutyrate also inhibits the synthesis of proteins and enzymes, although it does not inhibit DNA replication or transcription.Formula:C12H14O3Purity:Min. 95%Molecular weight:206.24 g/mol
