CAS 898767-10-7
:6-(3,4-dichlorophenyl)-6-oxo-hexanoic acid
Description:
6-(3,4-Dichlorophenyl)-6-oxo-hexanoic acid is a chemical compound characterized by its unique structure, which includes a hexanoic acid backbone with a ketone functional group and a dichlorophenyl substituent. The presence of the 3,4-dichlorophenyl group indicates that the compound has two chlorine atoms attached to the aromatic ring, which can influence its reactivity and biological activity. This compound is likely to exhibit moderate to high lipophilicity due to the aromatic ring, which can affect its solubility in organic solvents and its interaction with biological membranes. The carboxylic acid functional group contributes to its acidity and potential for forming salts or esters. Additionally, the compound may have applications in pharmaceuticals or agrochemicals, given the structural motifs often associated with bioactive molecules. Its specific properties, such as melting point, boiling point, and reactivity, would require experimental determination or detailed literature references for precise characterization.
Formula:C12H12Cl2O3
InChI:InChI=1/C12H12Cl2O3/c13-9-6-5-8(7-10(9)14)11(15)3-1-2-4-12(16)17/h5-7H,1-4H2,(H,16,17)
SMILES:C(CCC(=O)O)CC(=O)c1ccc(c(c1)Cl)Cl
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