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CAS 84182-48-9

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trans-3-(Phenylmethoxy)cyclobutanecarboxylic acid

Description:
Trans-3-(Phenylmethoxy)cyclobutanecarboxylic acid is an organic compound characterized by its cyclobutane ring structure, which is a four-membered carbon ring. The presence of a phenylmethoxy group indicates that there is a phenyl group attached to a methoxy group, contributing to the compound's overall hydrophobic character. The carboxylic acid functional group (-COOH) imparts acidic properties, allowing the compound to participate in various chemical reactions, such as esterification and amidation. This compound may exhibit chirality due to the presence of stereogenic centers, which can influence its biological activity and interactions. Its structural features suggest potential applications in pharmaceuticals or as intermediates in organic synthesis. The compound's solubility, stability, and reactivity can vary based on environmental conditions such as pH and temperature. Overall, trans-3-(Phenylmethoxy)cyclobutanecarboxylic acid is a versatile compound with unique characteristics that make it of interest in both academic and industrial chemistry contexts.
Formula:C12H14O3
InChI:InChI=1/C12H14O3/c13-12(14)10-6-11(7-10)15-8-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2,(H,13,14)/t10-,11-
InChI key:InChIKey=YNNOFVDQHAHVFG-XYPYZODXNA-N
SMILES:O(CC1=CC=CC=C1)[C@H]2C[C@H](C(O)=O)C2
Synonyms:
  • trans-3-(Phenylmethoxy)cyclobutanecarboxylic acid
  • trans-3-(Benzyloxy)cyclobutanecarboxylic acid
  • Cyclobutanecarboxylic acid, 3-(phenylmethoxy)-, trans-
  • trans-3-Phenylmethoxy-1-cyclobutanecarboxylic acid
  • (1r,3r)-3-(benzyloxy)cyclobutane-1-carboxylic acid
  • trans-3-Phenylmethoxy-1-cyclobutanecarboxylic acid - [P13204]
  • trans-3-Benzyloxycyclobutanecarboxylic acid
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