CAS 61008-98-8
:(2R)-(3-chlorophenyl)(hydroxy)ethanoic acid
Description:
(2R)-(3-chlorophenyl)(hydroxy)ethanoic acid, also known as a derivative of phenylacetic acid, is characterized by its specific stereochemistry and functional groups. This compound features a chiral center at the second carbon, which contributes to its enantiomeric properties. The presence of a hydroxyl group (-OH) and a carboxylic acid group (-COOH) indicates that it is an acidic compound, capable of donating protons in solution. The 3-chlorophenyl group enhances its lipophilicity and may influence its biological activity, making it relevant in pharmaceutical applications. The chlorinated aromatic ring can also affect the compound's reactivity and interaction with biological targets. Additionally, the compound's solubility, stability, and reactivity can vary based on pH and solvent conditions. Overall, this substance is of interest in medicinal chemistry and may exhibit specific pharmacological effects due to its structural features.
Formula:C8H7ClO3
InChI:InChI=1/C8H7ClO3/c9-6-3-1-2-5(4-6)7(10)8(11)12/h1-4,7,10H,(H,11,12)/t7-/m1/s1
SMILES:c1cc(cc(c1)Cl)[C@H](C(=O)O)O
Synonyms:- 61008-98-8
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Found 4 products.
(R)-()-3-Chloromandelic acid
CAS:Formula:C8H7ClO3Purity:98%Color and Shape:SolidMolecular weight:186.5924(R)-2-(3-Chlorophenyl)-2-hydroxyacetic acid
CAS:(R)-2-(3-Chlorophenyl)-2-hydroxyacetic acidPurity:98%Molecular weight:186.59g/mol(R)-2-(3-CHLOROPHENYL)-2-HYDROXYACETIC ACID
CAS:Formula:C8H7ClO3Purity:98%Color and Shape:SolidMolecular weight:186.59(R)-(-)-3-Chloromandelic Acid
CAS:Controlled Product<p>Applications (R)-(-)-3-Chloromandelic Acid is a reagent used in asymmetric syntheses due to its chirality. Used in the synthesis of a fluorescent analog of phenytoin as an inhibitor of neuropathic pain.<br>References Walls, T. et al.: Bioorg. Med. Chem., 20, 5269 (2012);<br></p>Formula:C8H7ClO3Color and Shape:NeatMolecular weight:186.59



