The chemical substance known as (2E)-3-[3-(3-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]prop-2-enoic acid, with the CAS number 372107-21-6, is characterized by its complex molecular structure, which includes a pyrazole ring and a bromophenyl group. This compound features a prop-2-enoic acid moiety, indicating it has both an alkene and a carboxylic acid functional group. The presence of the bromine atom in the phenyl ring contributes to its potential reactivity and biological activity, as halogenated compounds often exhibit unique properties. The compound's configuration as (2E) suggests a specific geometric arrangement around the double bond, which can influence its interactions and stability. It may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential applications in medicinal chemistry or as a building block in organic synthesis. The presence of multiple aromatic systems may also suggest potential for π-π stacking interactions, which can be relevant in biological contexts.

(2E)-3-[3-(3-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]prop-2-enoic acid

372107-21-6: The chemical substance known as (2E)-3-[3-(3-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]prop-2-enoic acid, with the CAS number 372107-21-6, is characterized by its complex molecular structure, which includes a pyrazole ring and a bromophenyl group. This compound features a prop-2-enoic acid moiety, indicating it has both an alkene and a carboxylic acid functional group. The presence of the bromine atom in the phenyl ring contributes to its potential reactivity and biological activity, as halogenated compounds often exhibit unique properties. The compound's configuration as (2E) suggests a specific geometric arrangement around the double bond, which can influence its interactions and stability. It may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential applications in medicinal chemistry or as a building block in organic synthesis. The presence of multiple aromatic systems may also suggest potential for π-π stacking interactions, which can be relevant in biological contexts.

CAS 372107-21-6

(2E)-3-[3-(3-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]prop-2-enoic acid

(2E)-3-[3-(3-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]acrylic acid

Ref: 10-F314623

(E)-3-(3-(3-Bromophenyl)-1-phenyl-1H-pyrazol-4-yl)acrylic acid

Ref: IN-DA00C88A