1017080-47-5

Basic information

• Product Name: 6-fluoro-3-(p-tolyl)-4H-chromen-4-one
• Synonyms: 6-fluoro-3-(p-tolyl)-4H-chromen-4-one
• CAS NO: 1017080-47-5
• Molecular Weight: 254.261
• Mol File: 1017080-47-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-fluoro-3-(p-tolyl)-4H-chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-fluoro-3-(p-tolyl)-4H-chromen-4-one(1017080-47-5)
• EPA Substance Registry System: 6-fluoro-3-(p-tolyl)-4H-chromen-4-one(1017080-47-5)

Safety Data

• Hazardous Substances Data: 1017080-47-5(Hazardous Substances Data)

Upstream product

• 475598-83-5 tris(4-fluorophenyl)sulfonium trifluoromethanesulfonate 
• 127820-38-6 tris(4-methylphenyl)sulfonium trifluoromethanesulfonate 
• 904318-52-1 (E)-3-(dimethylamino)-1-(5-fluoro-2-hydroxyphenyl)prop-2-en-1-one 
• 60565-88-0 bis(4-methylphenyl)iodonium hexafluorophosphate 
• 123726-16-9 bis(4-methylphenyl)iodonium trifluoromethanesulfonate 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 454689-23-7 6-fluoro-3-iodo-4H-1-benzopyran-4-one 
• 5142-75-6 tri(p-tolyl)bismuth 

Downstream Products

• 1456626-66-6 3-cyano-6-(5-fluoro-2-hydroxyphenyl)-5-(4-methylphenyl)pyridin-2(1H)-one 
• 1427272-64-7 3-cyano-6-(5-fluoro-2-hydroxylphenyl)-5-(4-methylphenyl)-pyridine-2(1H)-thione 

Relevant articles and documents

Arylation of ortho-Hydroxyarylenaminones by Sulfonium Salts and Arenesulfonyl Chlorides: An Access to Isoflavones

Herein we disclose three new methods for the straightforward and efficient synthesis of 3-arylchromones following the arylation of ortho-hydroxyarylenaminones by vast diversities of bench-stable and easy-to-use sulfonium salts and arenesulfonyl chlorides.

Pd-Catalyzed efficient cross-couplings of 3-iodochromones with triarylbismuths as substoichiometric multicoupling organometallic nucleophiles

An efficient cross-coupling of 3-iodochromones with triarylbismuths under catalytic palladium conditions is reported. Triarylbismuths were employed as substoichiometric multicoupling nucleophiles for the synthesis of a variety of substituted isoflavones.