(4-Chlorophenyl)acetaldehyde, with the CAS number 4251-65-4, is an organic compound characterized by the presence of a chlorophenyl group attached to an acetaldehyde moiety. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic chlorophenyl structure. The presence of the chlorine atom enhances its reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. (4-Chlorophenyl)acetaldehyde can undergo typical aldehyde reactions, including oxidation and condensation, and may participate in electrophilic aromatic substitution due to the electron-withdrawing nature of the chlorine substituent. Safety precautions should be observed when handling this compound, as it may pose health risks through inhalation or skin contact. Overall, its unique structural features and reactivity profile make it a valuable intermediate in organic synthesis.

(4-Chlorophenyl)acetaldehyde

4251-65-4: (4-Chlorophenyl)acetaldehyde, with the CAS number 4251-65-4, is an organic compound characterized by the presence of a chlorophenyl group attached to an acetaldehyde moiety. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic chlorophenyl structure. The presence of the chlorine atom enhances its reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. (4-Chlorophenyl)acetaldehyde can undergo typical aldehyde reactions, including oxidation and condensation, and may participate in electrophilic aromatic substitution due to the electron-withdrawing nature of the chlorine substituent. Safety precautions should be observed when handling this compound, as it may pose health risks through inhalation or skin contact. Overall, its unique structural features and reactivity profile make it a valuable intermediate in organic synthesis.

CAS 4251-65-4

(4-Chlorophenyl)acetaldehyde

2-(4-chlorophenyl)acetaldehyde

Ref: 54-OR927834

(4-CHLORO-PHENYL)-ACETALDEHYDE

Ref: IN-DA00BXIH

(4-Chlorophenyl)acetaldehyde

Ref: IN-DG28705

(4-Chlorophenyl)acetaldehyde

Ref: 10-F065182