37770-89-1

Upstream product

• 17422-74-1 3-Formylchromone 

Downstream Products

• 1624821-55-1 3-[4-(2-isopropyl-phenyl)-3,6-dihydro-2H-pyridin-1-ylmethyl]-chromen-4-one 
• 1186311-31-8 Br^(1-)*C₂₈H₂₂O₂P⁽¹⁺⁾ 
• 71972-61-7 3-(4-hydroxybenzyl)-4H-chromen-4-one 
• 153650-31-8 3-(2-hydroxybenzyl)-6-methyl<1>benzopyran-4-one 
• 63154-83-6 3-(2-hydroxybenzyl)<1>benzopyran-4-one 

Relevant academic research and scientific papers

Transformations of 4-oxo-4H-chromene-3-carbaldehyde under the action of FE(CO)5

Transformations of 4-oxo-4H-chromene-3-carbaldehyde in the presence of pentacarbonyliron and HMPA in benzene and toluene were studied, and their probable mechanism was proposed. The structure of 3-(4-oxochroman-3-ylmethyl)- 4H-chromen-4-one was determined by spectral methods and X-ray analysis. Pleiades Publishing, Ltd., 2012.

Benzopyrans : Part 40 - Alumina mediated transformations of 4-oxo-4H-1- benzopyran-3-carbaldehyde, -3-carboxylic acid and their 2-methylhomologues

In contact with alumina, the title aldehyde 1 (R = H, Me, Cl) gives the chromones 5 and 9,12 whereas the acid 2 affords the chromones 7, 10 and acetophenone 23. Alumina converts the aldehyde 3 to the xanthone 14, and the corresponding acid 4 to the chromone 8 and diketone 24.