107572-07-6 | 2-(4-Chlorophenylthio)benzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$30.00	$21.00

Description

• Catalog Number: AB59060
• Chemical Name: 2-(4-Chlorophenylthio)benzaldehyde
• CAS Number: 107572-07-6
• Molecular Formula: C13H9ClOS
• Molecular Weight: 248.728
• MDL Number: MFCD00051766
• SMILES: O=Cc1ccccc1Sc1ccc(cc1)Cl

Upstream Synthesis Route

2-((4-Chlorophenyl)thio)benzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactions. In organic chemistry, this compound serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials.One of the primary applications of 2-((4-Chlorophenyl)thio)benzaldehyde is as a starting material for the synthesis of heterocyclic compounds. By reacting with different reagents and catalysts, it can be transformed into a wide range of functionalized compounds, such as thiazoles, quinolines, and benzothiazoles. These heterocyclic structures are essential in the development of new drugs, polymers, and dyes.Additionally, 2-((4-Chlorophenyl)thio)benzaldehyde plays a crucial role in the preparation of various sulfur-containing compounds. Its thioether group allows for the formation of sulfides, sulfoxides, and sulfones through oxidation or substitution reactions. These sulfur-containing compounds are important in medicinal chemistry, as they exhibit diverse biological activities and can act as enzyme inhibitors or antimicrobial agents.Furthermore, the benzaldehyde moiety in 2-((4-Chlorophenyl)thio)benzaldehyde is a valuable functional group that can undergo numerous chemical transformations, such as condensation reactions, reduction, and oxidation. This enables chemists to modify the structure of the compound and introduce different substituents for targeted applications.Overall, 2-((4-Chlorophenyl)thio)benzaldehyde is a versatile compound with significant potential in chemical synthesis, particularly in the development of biologically active molecules and functional materials. Its diverse reactivity and ability to participate in various reactions make it a valuable asset in the toolkit of synthetic chemists.