1315334-84-9

Basic information

• Product Name: tert-butyl (2R,3S)-4-oxo-3-(3-oxobutyl)-2-phenylchroman-3-carboxylate
• Synonyms: tert-butyl (2R,3S)-4-oxo-3-(3-oxobutyl)-2-phenylchroman-3-carboxylate
• CAS NO: 1315334-84-9
• Molecular Weight: 394.467
• Mol File: 1315334-84-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (2R,3S)-4-oxo-3-(3-oxobutyl)-2-phenylchroman-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2R,3S)-4-oxo-3-(3-oxobutyl)-2-phenylchroman-3-carboxylate(1315334-84-9)
• EPA Substance Registry System: tert-butyl (2R,3S)-4-oxo-3-(3-oxobutyl)-2-phenylchroman-3-carboxylate(1315334-84-9)

Safety Data

• Hazardous Substances Data: 1315334-84-9(Hazardous Substances Data)

Upstream product

• 78-94-4 methyl vinyl ketone 
• 936183-32-3 tert-butyl (E)-2-(2-hydroxyphenylcarbonyl)-3-phenylprop-2-enoate 

Relevant articles and documents

Tandem intramolecular oxa-Michael addition/decarboxylation reaction catalyzed by bifunctional cinchona alkaloids: Facile synthesis of chiral flavanone derivatives

Bifunctional cinchona alkaloids were used to catalyze a tandem intramolecular oxa-Michael addition/decarboxylation reaction of alkylidene β-ketoesters 1, providing a series of flavanone derivatives with up to 97% yield and 93% ee.