3-(4-Chlorophenyl)-2-phenylprop-2-enoic acid, also known by its CAS number 7466-99-1, is an organic compound characterized by its structure, which features a prop-2-enoic acid backbone substituted with a 4-chlorophenyl group and a phenyl group. This compound typically exhibits properties associated with aromatic compounds, including potential hydrophobicity due to the presence of multiple aromatic rings. It is likely to be a solid at room temperature, with a relatively high melting point compared to aliphatic acids, owing to its complex structure and the presence of halogen substituents, which can influence its reactivity and solubility. The chlorophenyl group may impart specific electronic properties, affecting its reactivity in various chemical reactions, such as electrophilic substitutions or coupling reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis and applications would typically involve organic synthesis techniques, and it may be studied for its potential uses in medicinal chemistry or as an intermediate in the production of other chemical entities.

3-(4-chlorophenyl)-2-phenylprop-2-enoic acid

7466-99-1: 3-(4-Chlorophenyl)-2-phenylprop-2-enoic acid, also known by its CAS number 7466-99-1, is an organic compound characterized by its structure, which features a prop-2-enoic acid backbone substituted with a 4-chlorophenyl group and a phenyl group. This compound typically exhibits properties associated with aromatic compounds, including potential hydrophobicity due to the presence of multiple aromatic rings. It is likely to be a solid at room temperature, with a relatively high melting point compared to aliphatic acids, owing to its complex structure and the presence of halogen substituents, which can influence its reactivity and solubility. The chlorophenyl group may impart specific electronic properties, affecting its reactivity in various chemical reactions, such as electrophilic substitutions or coupling reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis and applications would typically involve organic synthesis techniques, and it may be studied for its potential uses in medicinal chemistry or as an intermediate in the production of other chemical entities.

4-Chloro-(alpha-phenyl)-cinnamic acid is a fine chemical that is useful as a building block for research chemicals, reagents and speciality chemicals. It is also a versatile intermediate for the synthesis of complex compounds and a useful scaffold for the synthesis of high quality products. This compound can be used in reactions such as Friedel-Crafts acylation, nitration, amination, esterification and cyclization.

CAS 7466-99-1

3-(4-chlorophenyl)-2-phenylprop-2-enoic acid

4-Chloro-(α-phenyl)-cinnamic acid

Ref: 3D-FC66675