1-(3,4-Dichlorophenyl)-2,2-dimethylpropan-1-one, with the CAS number 854891-91-1, is an organic compound characterized by its ketone functional group and a complex aromatic structure. It features a dichlorophenyl group, which contributes to its chemical reactivity and potential biological activity. The presence of two methyl groups on the carbon adjacent to the carbonyl enhances its steric hindrance, influencing its physical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic aromatic ring. Its dichlorophenyl moiety suggests potential applications in pharmaceuticals or agrochemicals, as chlorinated aromatic compounds often possess significant biological activity. Safety data should be consulted, as chlorinated compounds can pose environmental and health risks. Overall, this compound's unique structure and functional groups make it of interest in various chemical research fields, particularly in the synthesis of more complex molecules or as a potential lead compound in drug development.

1-(3,4-dichlorophenyl)-2,2-dimethylpropan-1-one

854891-91-1: 1-(3,4-Dichlorophenyl)-2,2-dimethylpropan-1-one, with the CAS number 854891-91-1, is an organic compound characterized by its ketone functional group and a complex aromatic structure. It features a dichlorophenyl group, which contributes to its chemical reactivity and potential biological activity. The presence of two methyl groups on the carbon adjacent to the carbonyl enhances its steric hindrance, influencing its physical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic aromatic ring. Its dichlorophenyl moiety suggests potential applications in pharmaceuticals or agrochemicals, as chlorinated aromatic compounds often possess significant biological activity. Safety data should be consulted, as chlorinated compounds can pose environmental and health risks. Overall, this compound's unique structure and functional groups make it of interest in various chemical research fields, particularly in the synthesis of more complex molecules or as a potential lead compound in drug development.

CAS 854891-91-1

1-(3,4-dichlorophenyl)-2,2-dimethylpropan-1-one

3′,4′-Dichloro-2,2-dimethylpropiophenone

Ref: 10-F204005