2-Chloro-1-(pentamethylphenyl)ethanone, with the CAS number 57196-63-1, is an organic compound characterized by its ketone functional group and the presence of a chlorine atom. This compound features a pentamethylphenyl group, which indicates a highly substituted aromatic ring, contributing to its unique chemical properties. The presence of the chlorine atom enhances its reactivity, making it useful in various synthetic applications. Typically, compounds like this exhibit moderate to high stability under standard conditions but may undergo reactions such as nucleophilic substitution or electrophilic aromatic substitution due to the electron-withdrawing nature of the carbonyl and chlorine groups. Its physical properties, such as boiling point and solubility, can vary based on the molecular structure and substituents. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, where specific reactivity and functionalization are required. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

2-chloro-1-(pentamethylphenyl)ethanone

57196-63-1: 2-Chloro-1-(pentamethylphenyl)ethanone, with the CAS number 57196-63-1, is an organic compound characterized by its ketone functional group and the presence of a chlorine atom. This compound features a pentamethylphenyl group, which indicates a highly substituted aromatic ring, contributing to its unique chemical properties. The presence of the chlorine atom enhances its reactivity, making it useful in various synthetic applications. Typically, compounds like this exhibit moderate to high stability under standard conditions but may undergo reactions such as nucleophilic substitution or electrophilic aromatic substitution due to the electron-withdrawing nature of the carbonyl and chlorine groups. Its physical properties, such as boiling point and solubility, can vary based on the molecular structure and substituents. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, where specific reactivity and functionalization are required. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

CAS 57196-63-1

2-chloro-1-(pentamethylphenyl)ethanone

2,3,4,5,6-Pentamethylphenacyl chloride

Ref: 54-OR23406

2-Chloro-1-(pentamethylphenyl)ethanone

Ref: 3D-HCA19663