1489240-28-9

Basic information

• Product Name: C₃₃H₃₃NO₆
• Synonyms: C₃₃H₃₃NO₆
• CAS NO: 1489240-28-9
• Molecular Weight: 539.628
• Mol File: 1489240-28-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₃H₃₃NO₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₃₃NO₆(1489240-28-9)
• EPA Substance Registry System: C₃₃H₃₃NO₆(1489240-28-9)

Safety Data

• Hazardous Substances Data: 1489240-28-9(Hazardous Substances Data)

Upstream product

• 479423-32-0 tert-butyl (naphthalen-2-yl(phenylsulfonyl)methyl)carbamate 
• 15014-25-2 malonic acid dibenzyl ester 
• 1396512-33-6 1-(phenylethynyl)naphthalen-2-ol 
• 479423-45-5 tert-butyl naphthalen-2-ylmethylenecarbamate 

Relevant articles and documents

Asymmetric Mannich Reaction and Construction of Axially Chiral Sulfone-Containing Styrenes in One Pot from α-Amido Sulfones Based on the Waste-Reuse Strategy

A simultaneous asymmetric Mannich reaction and the construction of axially chiral sulfone-containing styrenes in one pot from α-amido sulfones based on the waste-reuse strategy was demonstrated. A series of chiral β-amino diesters and axially chiral sulfone-containing styrenes with various functional groups were synthesized in good to excellent yields and enantioselectivities under mild conditions. In addition, this protocol has been successfully applied to synthesize the anti-HIV drug Maraviroc and chiral trichloro derivatives.

Highly enantioselective synthesis of N-Protected β-Amino malonates catalyzed by magnetically separable heterogeneous rosin-derived amino thiourea catalysts: A Stereocontrolled Approach to β-Amino Acids

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