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CAS 62462-05-9

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methyl 5-methoxy-3-oxovalerate

Description:
Methyl 5-methoxy-3-oxovalerate, with the CAS number 62462-05-9, is an organic compound characterized by its ester functional group, which is typical of methyl esters. This compound features a methoxy group (-OCH3) and a ketone functional group (C=O) within its structure, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid, exhibiting moderate solubility in organic solvents due to its polar functional groups. The presence of the methoxy group enhances its lipophilicity, making it useful in various chemical reactions, including esterification and condensation reactions. Methyl 5-methoxy-3-oxovalerate may also serve as an intermediate in the synthesis of more complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its stability and reactivity can be influenced by environmental factors such as temperature and pH, which are important considerations in its handling and application. As with many organic compounds, safety data should be consulted to ensure proper handling and usage.
Formula:C7H12O4
InChI:InChI=1/C7H12O4/c1-10-4-3-6(8)5-7(9)11-2/h3-5H2,1-2H3
InChI key:InChIKey=OPURNNHYTATPKM-UHFFFAOYSA-N
SMILES:COCCC(=O)CC(=O)OC
Synonyms:
  • 5-Methoxy-3-oxopentanoic acid methyl ester
  • 5-Methoxy-3-oxovaleric acid methyl ester
  • Methyl 5-Methoxy-3-Oxopentanoate
  • Pentanoic acid, 5-methoxy-3-oxo-, methyl ester
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