3-Formylchromone
Electrospray ionization mass spectrometry (ESI-MS) of protonated 3-formylchromone (3-FC) shows loss of H2 as a major fragmentation route to yield a ketene cation, which on reaction with water forms a protonated carboxylic acid. The invivo salubrious effects of 3-FC against nitrosodiethylamine (NDEA) mediated early hepatocellular carcinogenesis has been investigated. Synthesis and characterization of 3-FC and its derivatives has been reported.
| Catalog Number | CBB1114100 |
| Alternative Name(s) | 4-Oxo-4H-1-benzopyran-3-carboxaldehyde |
| Molecular Formula | C10H6O3 |
| CAS# | 17422-74-1 |
| Purity | >97% |
| Inchi | 1S/C10H6O3/c11-5-7-6-13-9-4-2-1-3-8(9)10(7)12/h1-6H |
| Inchi Key | FSMYWBQIMDSGQP-UHFFFAOYSA-N |
| SMILES | O=CC1=COc2ccccc2C1=O |
| Size | Inquiry |
| Supplier Page | https://www.amerigoscientific.com/3-formylchromone-item-114100.html |
