One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 3-Methylbenzofuran-2-carbaldehyde, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1199-07-1, Name is 3-Methylbenzofuran-2-carbaldehyde, molecular formula is C10H8O2
Synthesis and spectroscopic properties of benzo- and naphthofuryl-3-hydroxychromones
With the focus of designing new fluorescent probes, four new 3-hydroxy-chromone derivatives bearing benzofuran and naphthofuran groups were synthesized. They show bathochromic absorption shifts relative to 3-hydroxyflavone with the ability of retention to display the excited-state proton transfer. Disruption of the planarity by the methyl group in the furan ring leads to a decrease of both the extinction coefficient and the contribution of long wavelength absorption band, while molecules without a methyl group showed two distinct absorption bands. Shifts to longer wavelengths are also observed in fluorescent spectra, and the absence of the methyl group results in a dramatic increase of fluorescence quantum yield and lifetime. Of the extended 3-hydroxychromone derivatives, 3-hydroxy-2-naphtho[2,1-b]furan-2-yl-chromone has shown comparable, and in some cases better, absorption and fluorescence properties than the 3-hydroxychromones synthesized so far, which make it a highly promising candidate as molecular probe for analytical chemistry, biophysics, and cellular biology.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of 3-Methylbenzofuran-2-carbaldehyde, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 1199-07-1
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H1571O – PubChem