The chemical substance known as (2-chlorophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)methanone, with the CAS number 164526-07-2, is a synthetic organic compound characterized by its complex structure, which includes a chlorophenyl group and a benzodioxin moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and stability. It may display moderate to high lipophilicity due to the presence of aromatic rings, which can influence its solubility in organic solvents. The chlorophenyl group can impart specific electronic effects, potentially affecting the compound's reactivity and interaction with biological targets. Additionally, the presence of the benzodioxin structure may suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. As with many organic compounds, its behavior in various chemical environments, including reactions with nucleophiles or electrophiles, will depend on the specific functional groups and steric factors present in its structure. Safety and handling precautions should be observed, as with all chemical substances.

(2-chlorophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)methanone

164526-07-2: The chemical substance known as (2-chlorophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)methanone, with the CAS number 164526-07-2, is a synthetic organic compound characterized by its complex structure, which includes a chlorophenyl group and a benzodioxin moiety. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and stability. It may display moderate to high lipophilicity due to the presence of aromatic rings, which can influence its solubility in organic solvents. The chlorophenyl group can impart specific electronic effects, potentially affecting the compound's reactivity and interaction with biological targets. Additionally, the presence of the benzodioxin structure may suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. As with many organic compounds, its behavior in various chemical environments, including reactions with nucleophiles or electrophiles, will depend on the specific functional groups and steric factors present in its structure. Safety and handling precautions should be observed, as with all chemical substances.

CAS 164526-07-2

(2-chlorophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)methanone

2-Chloro-3',4'-(ethylenedioxy)benzophenone

Ref: IN-DA001UXT

2-Chloro-3',4'-(ethylenedioxy)benzophenone

Ref: 10-F202080

6-(2-Chlorobenzoyl)-2,3-dihydro-1,4-benzodioxine

Ref: 3D-PGA52607