2-Chlorochalcone is an organic compound that belongs to the chalcone family, characterized by its structure, which consists of a phenyl group connected to an α,β-unsaturated carbonyl system. It features a chlorine atom substituted at the second position of the aromatic ring. This compound typically appears as a yellow to light brown solid and is known for its potential biological activities, including antimicrobial and anti-inflammatory properties. 2-Chlorochalcone is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the carbonyl group, making it a suitable candidate for further chemical modifications, such as reactions with nucleophiles. Additionally, the chlorine substituent can enhance the compound's lipophilicity, affecting its solubility and biological interactions. As with many organic compounds, safety precautions should be observed when handling 2-Chlorochalcone, as it may pose health risks if ingested or inhaled.

2-Chlorochalcone

3300-67-2: 2-Chlorochalcone is an organic compound that belongs to the chalcone family, characterized by its structure, which consists of a phenyl group connected to an α,β-unsaturated carbonyl system. It features a chlorine atom substituted at the second position of the aromatic ring. This compound typically appears as a yellow to light brown solid and is known for its potential biological activities, including antimicrobial and anti-inflammatory properties. 2-Chlorochalcone is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the carbonyl group, making it a suitable candidate for further chemical modifications, such as reactions with nucleophiles. Additionally, the chlorine substituent can enhance the compound's lipophilicity, affecting its solubility and biological interactions. As with many organic compounds, safety precautions should be observed when handling 2-Chlorochalcone, as it may pose health risks if ingested or inhaled.

<p>3-(2-Chlorophenyl)-1-phenylpropene-1-one is an amide that is synthesized by the acylation of 3-phenylpropene-1-one with 2,3,5,6-tetrafluorobenzoyl chloride in the presence of a base. The proton transport mechanism is initiated by the addition of a proton to the carbonyl group and then proceeds through an intermediate called a chalcone. This reaction can be accomplished using biomimetic methods or by using chalcones and halides as intermediates.</p>

CAS 3300-67-2

2-Chlorochalcone

3-(2-Chlorophenyl)-1-phenylpropene-1-one

Ref: 3D-FC145666