110466-18-7

Basic information

• Product Name: benzaldehyde dicyclohexyldithioacetal
• Synonyms: benzaldehyde dicyclohexyldithioacetal
• CAS NO: 110466-18-7
• Molecular Weight: 320.563
• Mol File: 110466-18-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: benzaldehyde dicyclohexyldithioacetal(CAS DataBase Reference)
• NIST Chemistry Reference: benzaldehyde dicyclohexyldithioacetal(110466-18-7)
• EPA Substance Registry System: benzaldehyde dicyclohexyldithioacetal(110466-18-7)

Safety Data

• Hazardous Substances Data: 110466-18-7(Hazardous Substances Data)

Upstream product

• 1569-69-3 Cyclohexanethiol 
• 100-52-7 benzaldehyde 
• 106-54-7 p-Chlorothiophenol 
• 123290-13-1 phenyltriisopropylsilylmethanone 
• 132868-67-8 (tert-butyldimethylsilyl)(phenyl)methanone 
• 63935-93-3 benzoyltriethylsilane 

Relevant articles and documents

Neutral lithium triflate (LiOTf) efficiently catalyzes chemoselective preparations of cyclic and acyclic dithioacetals from carbonyl compounds, acylals, and O,O-cyclic and open-chain acetals under solvent-free conditions

An efficient and chemoselective preparation of cyclic and acyclic thioacetals from carbonyl compounds, cyclic and acyclic acetals and acylals in the presence of catalytic amounts of neutral lithium triflate and thiols under solvent-free conditions is described.

Visible-Light Photoredox-Catalyzed Thioacetalization of Aldehydes Under Metal-Free and Solvent-Free Conditions

A first visible-light photoredox-catalyzed thioacetalization of aldehydes under metal-free and solvent-free conditions is described. Under blue LED irradiation, a reactive thiyl radical was initially generated through single-electron oxidation of thiol, w

Lithium bromide-catalyzed highly chemoselective and efficient dithioacetalization of α,β-unsaturated and aromatic aldehydes under solvent-free conditions

Chemoselective dithioacetalization of aromatic- and α,β- unsaturated aldehydes in the presence of other structurally different aldehydes and ketones was achieved efficiently in the presence of catalytic amounts of LiBr under solvent-free conditions. Due to the neutral reaction conditions, this method is compatible with acid sensitive substrates.