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CAS 81025-83-4

:

(R)-4-Methoxy-2-methyl-4-oxobutanoic acid

Description:
(R)-4-Methoxy-2-methyl-4-oxobutanoic acid, with the CAS number 81025-83-4, is an organic compound characterized by its chiral structure, which includes a methoxy group and a ketone functional group. This compound features a four-carbon backbone with a carboxylic acid functional group, contributing to its acidic properties. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. As a chiral molecule, it exists in two enantiomeric forms, with the (R) configuration being one of them, which can have significant implications in pharmacology and biochemistry, as different enantiomers can exhibit different biological activities. The compound is likely to participate in various chemical reactions typical of carboxylic acids and ketones, such as esterification and oxidation. Its specific applications may vary, but it could be relevant in the synthesis of pharmaceuticals or as an intermediate in organic synthesis.
Formula:C6H10O4
InChI:InChI=1S/C6H10O4/c1-4(6(8)9)3-5(7)10-2/h4H,3H2,1-2H3,(H,8,9)/t4-/m1/s1
InChI key:InChIKey=UVQYBUYGFBXQGO-SCSAIBSYSA-N
SMILES:C([C@H](C(O)=O)C)C(OC)=O
Synonyms:
  • (2R)-4-methoxy-2-methyl-4-oxobutanoic acid
  • (R)-(+)-2-Methylsuccinic acid 4-methyl ester
  • (R)-(+)-3-Methylsuccinic acid 1-monomethyl ester
  • (R)-4-Methoxy-2-methyl-4-oxo-butanoic acid
  • (R)-4-Methoxy-2-methyl-4-oxobutanoic acid
  • Butanedioic acid, 2-methyl-, 4-methyl ester, (2R)-
  • Butanedioic acid, methyl-, 4-methyl ester, (2R)-
  • Butanedioic acid, methyl-, 4-methyl ester, (R)-
  • Methyl (R)-3-methylsuccinate
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