1256348-07-8

Basic information

• Product Name: C₁₉H₁₅ClS
• Synonyms: C₁₉H₁₅ClS
• CAS NO: 1256348-07-8
• Molecular Weight: 310.847
• Mol File: 1256348-07-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₉H₁₅ClS(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₁₅ClS(1256348-07-8)
• EPA Substance Registry System: C₁₉H₁₅ClS(1256348-07-8)

Safety Data

• Hazardous Substances Data: 1256348-07-8(Hazardous Substances Data)

Upstream product

• 196953-02-3 1-(4-chlorophenyl)buta-2,3-dien-1-one 
• 104-88-1 4-chlorobenzaldehyde 
• 42249-99-0 1-(4-chlorophenyl)but-3-yn-1-ol 
• 1256347-99-5 4-(4-chlorophenyl)hepta-1,2-dien-6-yn-4-ol 
• 108-98-5 thiophenol 

Relevant articles and documents

InI3- or ZnI2-catalyzed reaction of hydroxylated 1,5-allenynes with thiols: A new access to 3,5-disubstituted toluene derivatives

Transition-metal-activated alkynes or allenes can accept nucleophilic attack and undergo direct addition of the nucleophiles to the unsaturated bonds or trigger subsequent rearrangement reactions. This chemistry has witnessed increasing development in recent years. In this report, we have focused on the metal-catalyzed reactions of a variety of substituted propargyl allenic alcohols and thiophenols using indiumACHTUNGTRENUNG(III) and zinc(II) catalysts, which can activate both the alcohol and alkyne. In this reaction, thio groups play the role of a nucleophile and trigger subsequent rearrangements to give benzene derivatives. The products can be further transformed into various 1,3,5-trisubstituted aromatic compounds by nickel-catalyzed coupling reactions through the cleavage of the C-S bonds.