1536481-20-5

Basic information

• Product Name: (2R,3R)-4-(tert-butoxy)-1,3-dihydroxy-4-oxobutan-2-yl 2,6-dimethylbenzoate
• Synonyms: (2R,3R)-4-(tert-butoxy)-1,3-dihydroxy-4-oxobutan-2-yl 2,6-dimethylbenzoate
• CAS NO: 1536481-20-5
• Molecular Weight: 324.374
• Mol File: 1536481-20-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R)-4-(tert-butoxy)-1,3-dihydroxy-4-oxobutan-2-yl 2,6-dimethylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-4-(tert-butoxy)-1,3-dihydroxy-4-oxobutan-2-yl 2,6-dimethylbenzoate(1536481-20-5)
• EPA Substance Registry System: (2R,3R)-4-(tert-butoxy)-1,3-dihydroxy-4-oxobutan-2-yl 2,6-dimethylbenzoate(1536481-20-5)

Safety Data

• Hazardous Substances Data: 1536481-20-5(Hazardous Substances Data)

Upstream product

• 7633-32-1 tert-butyl glyoxylate 
• 1536481-30-7 2,6-dimethylbenzoyloxyacetaldehyde 
• 848821-76-1 (S)-(-)-α,α-bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol 

Relevant articles and documents

Amine-catalyzed asymmetric cross-aldol reactions using heterofunctionalized acetaldehydes as nucleophiles

Various heterofunctionalized acetaldehydes were successfully employed in an amine-catalyzed asymmetric cross-aldol reaction, affording a variety of synthetically useful 1,2-difunctionalized compounds such as 1,2-diols and 1,2-aminoalcohols. With this method, both syn- and anti-1,2-difunctionalized compounds were obtained from the same set of reactants by using the appropriate amine catalyst.