CAS 709-63-7
:4-(Trifluorometil)acetofenona
- (4-Trifluoromethylphenyl) methyl ketone
- 1-Acetyl-4-(trifluoromethyl)benzene
- 1-[4-(Trifluoromethyl)Phenyl]Ethanone
- 1-[4-(Trifluoromethyl)phenyl]-1-ethanone
- 2-Bromo-2,2-Difluoroethanamine
- 4-Acetylbenzotrifluoride
- Acetophenone, 4′-(trifluoromethyl)-
- Ethanone, 1-[4-(trifluoromethyl)phenyl]-
- Methyl 4-trifluoromethylphenyl ketone
- NSC 88346
- Sodium4-trifluoromethylbenzoate
- p-(Trifluoromethyl)acetophenone
- p-Trifluoromethylacetophenone
- 4'-(Trifluoromethyl)-Acetophenone
- 4'-(Trifluoromethyl)acetophenone
- 4[-(Trifluoromethyl)acetophenone
- 4-(Trifluoromethyl) acetophenone
- Ver mais sinónimos
4'-(Trifluoromethyl)acetophenone, 98+%
CAS: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 reference has not changed as a part of the brand transition to Thermo Sci
Fórmula:C9H7F3OPureza:98+%Cor e Forma:Crystals or powder or crystalline powder or fused solid, White to pale cream or pale yellowPeso molecular:188.151-(4-(Trifluoromethyl)phenyl)ethanone
CAS:Fórmula:C9H7F3OPureza:98%Cor e Forma:SolidPeso molecular:188.14654'-(Trifluoromethyl)acetophenone
CAS:4'-(Trifluoromethyl)acetophenoneFórmula:C9H7F3OPureza:≥95%Cor e Forma: clear. almost colourless to off white. low melting solid or liquidPeso molecular:188.15g/mol4'-(Trifluoromethyl)acetophenone
CAS:Fórmula:C9H7F3OPureza:>98.0%(GC)Cor e Forma:White or Colorless to Light yellow powder to lump to clear liquidPeso molecular:188.154′-(Trifluoromethyl)acetophenone
CAS:Fórmula:C9H7F3OPureza:98%Cor e Forma:Low Melting SolidPeso molecular:188.1494'-(Trifluoromethyl)acetophenone
CAS:4'-(Trifluoromethyl)acetophenone is a phosphatase inhibitor that has been shown to have inhibitory activity against chemokines. Chemokines are a type of cytokine that are secreted by immune cells and play an important role in inflammation. 4'-(Trifluoromethyl)acetophenone has also been shown to have an effect on the cell membrane permeability of amines and 2-aminobenzyl alcohol, which are substrates for the enzyme. 4'-(Trifluoromethyl)acetophenone reacts with imidazole derivatives, such as trifluoride, forming hydrogen bonds between the two molecules. Kinetic studies have demonstrated that this reaction is reversible in solution at room temperature.
Fórmula:C9H7F3OPureza:Min. 95%Cor e Forma:PowderPeso molecular:188.15 g/molRef: 3D-FT28471
Produto descontinuado






