135301-06-3

Upstream product

• 103-82-2 phenylacetic acid 
• 54246-38-7 1-(5-hydroxy-2H-chromen-6-yl)-ethanone 
• 55628-82-5 1-(Phenylacetyl)imidazole 
• 67091-10-5 1-(2-hydroxy-4-prop-2-ynyloxy-phenyl)-ethanone 
• 135301-04-1 4-methyl-3-phenyl-7-propargyloxycoumarin 

Relevant academic research and scientific papers

Microwave assisted synthesis of 4-methyl-3-arylpyrano[2,3-f]chromen-2(8H)-one derivatives, evaluation of antiproliferative, and antimicrobial activities

A series of new 4-methyl-3-arylpyrano[2,3-f]chromen-2(8H)-one derivatives were designed and synthesized through an efficient, an eco-friendly manner under microwave irradiation and conventional heating methods. Structures of final compounds established ba

Claisen rearrangement of 7-propargyloxycoumarins: Formation of pyrano and furanocoumarins

The Claisen rearrangement of 4-methyl-7-propargyloxycoumarins in N,N-dimethylaniline results in the formation of angular pyranocoumarins (3) in high yields (71-78percent) and linear pyranocoumarins (4) in low yields (8-12percent).The effect of solvent on the rearrangement has been examined.