1208-88-4 | 4-(Phenylthio)benzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$15.00	$11.00
5g	95%	in stock	$50.00	$35.00
10g	95%	in stock	$80.00	$56.00
25g	95%	in stock	$155.00	$109.00
100g	95%	in stock	$613.00	$429.00

Description

• Catalog Number: AE08717
• Chemical Name: 4-(Phenylthio)benzaldehyde
• CAS Number: 1208-88-4
• Molecular Formula: C13H10OS
• Molecular Weight: 214.2829
• MDL Number: MFCD01666578
• SMILES: O=Cc1ccc(cc1)Sc1ccccc1

Upstream Synthesis Route

4-(Phenylthio)benzaldehyde, a versatile compound widely used in chemical synthesis, plays a crucial role in various reactions and transformations. Its presence as a key building block in organic synthesis offers a range of applications in the creation of complex molecules and pharmaceutical intermediates.In organic chemistry, 4-(Phenylthio)benzaldehyde serves as a precursor for the synthesis of substituted benzaldehydes and related compounds. Its ability to undergo various chemical transformations, such as nucleophilic addition reactions, allows for the introduction of different functional groups onto the phenylthio group, expanding its utility in organic synthesis.One common application of 4-(Phenylthio)benzaldehyde is in the formation of thioether linkages. By reacting with nucleophiles bearing the appropriate functionality, this compound can participate in thiol-ene reactions to yield thioether derivatives. This reaction pathway is crucial in the construction of sulfur-containing compounds with diverse properties and applications.Furthermore, 4-(Phenylthio)benzaldehyde can be utilized in the preparation of heterocyclic compounds through cyclization reactions. Its aromatic ring system and thioether moiety can undergo cyclization under specific conditions, leading to the formation of heterocycles with potential biological activity.Overall, the strategic incorporation of 4-(Phenylthio)benzaldehyde in chemical synthesis enables the synthesis of structurally complex molecules and provides access to a wide array of functionalized compounds with valuable applications in medicinal chemistry, material science, and bioorganic chemistry.