1438763-08-6

Basic information

• Product Name: (R)-2,2,2-trifluoro-N-(3-(4-oxochroman-2-yl)phenyl)acetamide
• Synonyms: (R)-2,2,2-trifluoro-N-(3-(4-oxochroman-2-yl)phenyl)acetamide
• CAS NO: 1438763-08-6
• Molecular Weight: 335.282
• Mol File: 1438763-08-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2,2,2-trifluoro-N-(3-(4-oxochroman-2-yl)phenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2,2,2-trifluoro-N-(3-(4-oxochroman-2-yl)phenyl)acetamide(1438763-08-6)
• EPA Substance Registry System: (R)-2,2,2-trifluoro-N-(3-(4-oxochroman-2-yl)phenyl)acetamide(1438763-08-6)

Safety Data

• Hazardous Substances Data: 1438763-08-6(Hazardous Substances Data)

Upstream product

• 491-38-3 1-benzopyran-4(4H)-one 
• 88978-20-5 3-(2,2,2-trifluoroacetamido)phenylboronic acid 

Relevant articles and documents

Palladium-catalyzed asymmetric conjugate addition of arylboronic acids to heterocyclic acceptors

Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing a single catalyst system formed in situ from Pd(OCOCF3)2 and (S)-tBuPyOX. Notably, these reactions are performed in wet solvent under ambient atmosphere, and employ readily available arylboronic acids as the nucleophile, thus providing ready access to these asymmetric heterocycles (see scheme).