1393802-60-2

Basic information

• Product Name: (R)-1-(4-(tert-butyl)phenyl)-2-methyl-3-oxopropan-2-yl benzoate
• Synonyms: (R)-1-(4-(tert-butyl)phenyl)-2-methyl-3-oxopropan-2-yl benzoate
• CAS NO: 1393802-60-2
• Molecular Weight: 324.42
• Mol File: 1393802-60-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-1-(4-(tert-butyl)phenyl)-2-methyl-3-oxopropan-2-yl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-(4-(tert-butyl)phenyl)-2-methyl-3-oxopropan-2-yl benzoate(1393802-60-2)
• EPA Substance Registry System: (R)-1-(4-(tert-butyl)phenyl)-2-methyl-3-oxopropan-2-yl benzoate(1393802-60-2)

Safety Data

• Hazardous Substances Data: 1393802-60-2(Hazardous Substances Data)

Upstream product

• 80-54-6 lilial 
• 94-36-0 dibenzoyl peroxide 

Downstream Products

• 1393802-91-9 (R)-3-(4-(tert-butyl)phenyl)-2-hydroxy-2-methylpropyl benzoate 

Relevant articles and documents

Organocatalytic asymmetric α-benzoyloxylation of α-branched aldehydes and enals: A useful approach to oxygenated quaternary stereocenters

Direct asymmetric α-benzoyloxylation of α-branched aldehydes and α-branched enals via enamine and dienamine catalysis was used to construct quaternary oxygenated stereocenters with good yields and moderate to good enantioselectivity. This method uses an inexpensive and readily available cinchona alkaloid-derived primary amine as the catalyst, benzoyl peroxide as the oxygen source, and stoichiometric amounts of the aldehyde substrates, providing simple metal-free access to valuable protected 2-hydroxyaldehyde derivatives.