2-(4-Chlorophenylthio)benzaldehyde, with the CAS number 107572-07-6, is an organic compound characterized by the presence of both a benzaldehyde functional group and a thioether moiety. This compound features a chlorophenyl group attached to a sulfur atom, which is further connected to a benzaldehyde structure. It typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and ethanol. The presence of the chlorophenyl group imparts certain electronic properties, potentially influencing its reactivity and interactions in chemical reactions. This compound may be utilized in various synthetic applications, including the development of pharmaceuticals and agrochemicals, due to its unique structural features. Additionally, its reactivity can be attributed to the electrophilic nature of the aldehyde group, making it a candidate for nucleophilic attack in various organic transformations. Safety precautions should be observed when handling this compound, as it may pose health risks typical of aromatic compounds with halogen substituents.

2-(4-Chlorophenylthio)benzaldehyde

107572-07-6: 2-[(4-Chlorophenyl)thio]benzaldehyde, 2-[(4-Chlorophenyl)Sulfanyl]Benzaldehyde

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2-(4-Chlorophenylthio)benzaldehyde, 98%

2-[(4-Chlorophenyl)thio]benzaldehyde

2-(4-Chlorophenylthio)benzaldehyde is a heterocyclic compound with two aromatic rings. The molecule has been shown to have diverse and valuable applications in the field of biomolecular chemistry, including its use as an analogue for benzaldehyde in the synthesis of various biologically active molecules, such as the antibiotic erythromycin.

CAS 107572-07-6: 2-(4-Chlorophenylthio)benzaldehyde

2-(4-Chlorophenylthio)benzaldehyde, 98%

Ref: 02-A12852

2-[(4-Chlorophenyl)thio]benzaldehyde

Ref: 54-OR25197

2-(4-Chlorophenylthio)benzaldehyde

Ref: 3D-FC170043

2-((4-Chlorophenyl)thio)benzaldehyde

Ref: IN-DA003EVW

2-(4-Chlorophenylthio)benzaldehyde, 98%

Ref: 10-F340630