936182-96-6

Basic information

• Product Name: tert-butyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate
• Synonyms: tert-butyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate
• CAS NO: 936182-96-6
• Molecular Weight: 266.294
• Mol File: 936182-96-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate(936182-96-6)
• EPA Substance Registry System: tert-butyl 3-(2-hydroxy-4-methoxyphenyl)-3-oxopropanoate(936182-96-6)

Safety Data

• Hazardous Substances Data: 936182-96-6(Hazardous Substances Data)

Upstream product

• 540-88-5 acetic acid tert-butyl ester 
• 5446-02-6 4-methoxymethylsalicylate 

Downstream Products

• 936183-97-0 tert-butyl (E)-2-(2-hydroxy-4-methoxyphenylcarbonyl)-3-phenylprop-2-enoate 
• 21785-09-1 7-methoxyflavanone 

Relevant articles and documents

Catalytic enantioselective synthesis of flavanones and chromanones

The enantioselective synthesis of flavanones and chromanones is described. Bifunctional thiourea catalysts promote an asymmetric oxo-conjugate addition to a β-ketoester alkylidene in high yields with excellent enantioselectivity (80-94% ee) for aryl and alkyl substrates. Decarboxylation of the β-ketoester proceeds smoothly in a one-pot procedure to afford the enantioenriched flavanones and chromanones. Copyright

Catalytic enantioselective synthesis of flavanones and chromanones

Various chromanone, flavanone and abyssinone compounds as can be prepared enantioselectively using a chiral thiourea catalyst.