1383612-01-8

Basic information

• Product Name: 4-(tert-butyl)-2-(tert-butylthio)benzaldehyde
• Synonyms: 4-(tert-butyl)-2-(tert-butylthio)benzaldehyde
• CAS NO: 1383612-01-8
• Molecular Weight: 250.405
• Mol File: 1383612-01-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(tert-butyl)-2-(tert-butylthio)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(tert-butyl)-2-(tert-butylthio)benzaldehyde(1383612-01-8)
• EPA Substance Registry System: 4-(tert-butyl)-2-(tert-butylthio)benzaldehyde(1383612-01-8)

Safety Data

• Hazardous Substances Data: 1383612-01-8(Hazardous Substances Data)

Upstream product

• 75-66-1 2-methylpropan-2-thiol 
• 246139-77-5 2-bromo-4-(tert-butyl)benzaldehyde 
• 246139-76-4 2-bromo-1-(bromomethyl)-4-(tert-butyl)benzene 
• 61024-94-0 2-bromo-4-tert-butyl-1-methylbenzene 
• 98-51-1 4-tert-butyltoluene 

Downstream Products

• 1383611-42-4 (1R,2R)-N,N-bis[4-(tert-butyl)-2-(tert-butylthio)benzylidene]-1,2-cyclohexanediamine 

Relevant articles and documents

Asymmetric hydrogenation of ketones with H2 and ruthenium catalysts containing chiral tetradentate S2N2 ligands

Getting more for less: In the presence of H2 and a base, air- and moisture-tolerant RuII complexes catalyze the hydrogenation of ketones and aldehydes with excellent activity and chemoselectivity, and with enantioselectivity of up to 95 % under mild conditions. The ratio of substrate to catalyst can be lowered to 106:1. The reactions tolerate scale-up and can be carried out with almost no solvent. A base-free method is available for base-sensitive substrates. Copyright