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CAS 220353-93-5

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(1R,2R)-2-(3-Chloro-4-methylphenyl)cyclopropanecarboxylic acid

Description:
(1R,2R)-2-(3-Chloro-4-methylphenyl)cyclopropanecarboxylic acid is a chiral cyclopropane derivative characterized by its unique structural features. This compound contains a cyclopropane ring, which contributes to its rigidity and distinct stereochemistry, specifically in the (1R,2R) configuration. The presence of a carboxylic acid functional group (-COOH) indicates that it can participate in acid-base reactions and may exhibit acidic properties. The attached 3-chloro-4-methylphenyl group introduces additional reactivity and influences the compound's physical and chemical properties, such as solubility and boiling point. This compound may also exhibit biological activity, making it of interest in pharmaceutical research. Its chirality suggests that it may have different biological effects depending on the stereoisomer, which is crucial in drug development. Overall, (1R,2R)-2-(3-Chloro-4-methylphenyl)cyclopropanecarboxylic acid is a complex molecule with potential applications in medicinal chemistry and organic synthesis.
Formula:C11H11ClO2
InChI:InChI=1S/C11H11ClO2/c1-6-2-3-7(4-10(6)12)8-5-9(8)11(13)14/h2-4,8-9H,5H2,1H3,(H,13,14)/t8-,9+/m0/s1
InChI key:InChIKey=TXEJAIDZLJVGOF-DTWKUNHWSA-N
SMILES:C(O)(=O)[C@H]1[C@@H](C1)C2=CC(Cl)=C(C)C=C2
Synonyms:
  • Cyclopropanecarboxylic acid, 2-(3-chloro-4-methylphenyl)-, (1R,2R)-
  • (1R,2R)-2-(3-Chloro-4-methylphenyl)cyclopropanecarboxylic acid
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