1-Chloro-3-phenylacetone, with the CAS number 937-38-2, is an organic compound characterized by its structure, which features a chloro group and a phenylacetone moiety. It typically appears as a colorless to pale yellow liquid with a distinctive odor. This compound is known for its reactivity due to the presence of the chloro substituent, which can participate in nucleophilic substitution reactions. It is moderately soluble in organic solvents but has limited solubility in water. 1-Chloro-3-phenylacetone is primarily used in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. Its handling requires caution, as it may pose health risks if inhaled or absorbed through the skin. Additionally, it is important to store this compound in a cool, dry place away from incompatible materials to prevent any hazardous reactions. Overall, 1-chloro-3-phenylacetone is a valuable intermediate in chemical synthesis, with applications in various fields of chemistry.

1-Chloro-3-Phenylacetone

Chloromethyl ketone (CMK) is a reactive chemical that can be used to inactivate the active form of histidine-containing enzymes. It reacts with the basic group of histidine and forms an alkylating agent, which prevents the enzyme from functioning. CMK has been shown to affect ionophore transport in populations of bacteria and yeast cells. CMK also has bifunctional properties, as it can act as an ionophore or emulsifier. This chemical is sometimes used to create homologous protein structures for protein crystallization studies. The imidazole ring is hydrophobic and may be important for binding to proteins.

CAS 937-38-2: 1-Chloro-3-Phenylacetone

1-Chloro-3-phenyl-propan-2-one

Ref: 3D-FC170239

1-Chloro-3-phenylpropan-2-one

Ref: 10-F243266

1-CHLORO-3-PHENYLACETONE

Ref: IN-DA0061HD