1017080-36-2

Basic information

• Product Name: 6-methyl-3-(p-tolyl)-4H-chromen-4-one
• Synonyms: 6-methyl-3-(p-tolyl)-4H-chromen-4-one
• CAS NO: 1017080-36-2
• Molecular Weight: 250.297
• Mol File: 1017080-36-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-methyl-3-(p-tolyl)-4H-chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methyl-3-(p-tolyl)-4H-chromen-4-one(1017080-36-2)
• EPA Substance Registry System: 6-methyl-3-(p-tolyl)-4H-chromen-4-one(1017080-36-2)

Safety Data

• Hazardous Substances Data: 1017080-36-2(Hazardous Substances Data)

Upstream product

• 89807-39-6 1-(2-hydroxy-5-methylphenyl)-3-(N,N-dimethylamino)propenone 
• 127820-38-6 tris(4-methylphenyl)sulfonium trifluoromethanesulfonate 
• 98-59-9 p-toluenesulfonyl chloride 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 89807-39-6 (2E)-3-(dimethylamino)-1-(2-hydroxy-5-methylphenyl)-2-propen-1-one 
• 5142-75-6 tri(p-tolyl)bismuth 
• 341528-94-7 3-iodo-6-methyl-4H-chromen-4-one 

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.