CAS 4265-16-1
:2-Benzofurancarboxaldeído
- 1-Benzofuran-2-Carbaldehyde
- 2-Benzofurancarbaldehyde
- 2-Benzofurancarboxaldehyde
- 2-Formylbenzofuran
- Benzo[b]-2-furfural
- Benzo[b]furan-2-aldehyde
- Benzo[b]furan-2-carboxaldehyde
- Coumarilaldehyde
Benzo[b]furan-2-carboxaldehyde, 99%
CAS:Benzo[b]furan-2-carboxaldehyde is used for the synthesis of isoxazolines. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU
Fórmula:C9H6O2Pureza:99%Cor e Forma:Clear colorless to yellow, LiquidPeso molecular:146.15Benzo[b]furan-2-carboxaldehyde
CAS:Benzo[b]furan-2-carboxaldehyde is a CYP2A6 inhibitor and can be used in biochemical experiments and drug synthesis.Fórmula:C9H6O2Pureza:98.86%Cor e Forma:SolidPeso molecular:146.14Benzo[b]furan-2-carboxaldehyde
CAS:Benzo[b]furan-2-carboxaldehydeFórmula:C9H6O2Pureza:≥95%Cor e Forma: light yellow to yellow liquidPeso molecular:146.14g/molBenzofuran-2-carbaldehyde
CAS:Fórmula:C9H6O2Pureza:>98.0%(GC)Cor e Forma:Colorless to Yellow clear liquidPeso molecular:146.15Benzofuran-2-carboxaldehyde
CAS:Benzofuran-2-carboxaldehyde is a compound that inhibits metathesis reactions. It has been shown to inhibit the growth of cancer cells in vivo and in vitro. Benzofuran-2-carboxaldehyde also shows estrogen receptor modulator activity, which may be due to its ability to bind to estrogen receptors. The molecular modelling study of this compound reveals a possible mechanism for benzofuran-2-carboxaldehyde’s inhibition of metathesis reactions as well as its cytotoxicity. This mechanism suggests that the benzofuran-2-carboxaldehyde molecule can form hydrogen bonds with diphenyl ether and mcf7 cells, leading to their destabilization.
Fórmula:C9H6O2Pureza:Min. 95%Peso molecular:146.14 g/mol2-Benzofurancarboxaldehyde
CAS:Produto ControladoFórmula:C9H6O2Cor e Forma:NeatPeso molecular:146.143








