CAS 58914-34-4
:Benzaldeide, 2-idrossi-4-(trifluorometil)-
- 4-Trifluoromethylsalicyaldehyde
2-Formyl-5-(trifluoromethyl)phenol, 4-Formyl-3-hydroxybenzotrifluoride, 4-(Trifluoromethyl)salicylaldehyde
CAS:Formula:C8H5F3O2Purezza:98%Colore e forma:SolidPeso molecolare:190.11932-Hydroxy-4-(trifluoromethyl)benzaldehyde
CAS:2-Hydroxy-4-(trifluoromethyl)benzaldehydeFormula:C8H5F3O2Purezza:97%Colore e forma: faint lemon crystalsPeso molecolare:190.1193g/mol2-HYDROXY-4-(TRIFLUOROMETHYL)BENZALDEHYDE
CAS:Formula:C8H5F3O2Purezza:95%Colore e forma:SolidPeso molecolare:190.1212-Hydroxy-4-(trifluoromethyl)benzaldehyde
CAS:Prodotto controllatoFormula:C8H5F3O2Colore e forma:Colourless To Light YellowPeso molecolare:190.122-Hydroxy-4-(trifluoromethyl)benzaldehyde
CAS:2-Hydroxy-4-(trifluoromethyl)benzaldehyde is an analgesic and anti-inflammatory agent that belongs to the pyrazole family. It has shown analgesic and anti-inflammatory effects in animal studies. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been shown to be a potent inhibitor of cyclooxygenase (COX), which is responsible for prostaglandin synthesis, and as such, may have potential as a treatment for inflammatory conditions such as rheumatoid arthritis. This drug also inhibits the production of nitric oxide, which is involved in vasodilation and increased blood flow. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been demonstrated to inhibit COX enzymes by forming a covalent bond with active site serine residues on the enzyme. The docked complex shows hydrogen bonding interactions between the hydroxyl group of 2
Formula:C8H5F3O2Purezza:Min. 95%Peso molecolare:190.12 g/mol




