2-Bromo-4'-fluoroacetophenone

CAS: 403-29-2

Ref. 3D-FB35004

Produktinformation

• Name: 2-Bromo-4'-fluoroacetophenone
• Synonyme: 1-(4-Fluorophenyl)-2-bromoethanone, 2'-Bromo-4-Fluoroacetophenone, 2-Bromo-1-(4-Fluorophenyl)Ethanone, 2-Bromo-1-(4-fluorophenyl)-1-ethanone, 2-Bromo-4'-fluoro acetophentone, 2-Bromo-4'-fluoroacetophentone, 2-Bromo-p-fluoroacetophenone, 4-Fluorophenacyl bromide, 4′-Fluoro-2-bromoacetophenone, 4′-Fluoro-α-bromoacetophenone, Acetophenone, 2-bromo-4′-fluoro-, Bromo-4-fluoroacetophenone, Bromomethyl 4-fluorophenyl ketoxime, Buttpark 41\03-58, Ethanone, 2-bromo-1-(4-fluorophenyl)-, NSC 88343, P-Fluorophenacyl Bromide, Timtec-Bb Sbb006561, omega-Bromo-4-fluoroacetophenone, p-Fluoro-α-bromoacetophenone, α-Bromo-4-fluoroacetophenone, α-Bromo-p-fluoroacetophenone

Beschreibung

2-Bromo-4'-fluoroacetophenone is a synthetic chemical that has been shown to inhibit the growth of staphylococcus, anthranilic, and chromobacterium. It is also used in vivo assays as an inhibitor of carbonic anhydrase II. 2-Bromo-4'-fluoroacetophenone is used to inhibit hepg2 cells, which are cancer cells that produce human erythropoietin in vitro. It has been shown to have a quaternization effect on anhydrous sodium, which may reduce the potency of this chemical. It has also been found to be effective against stromal tumors and s. epidermidis bacteria.
The mechanism by which 2-bromo-4'-fluoroacetophenone inhibits bacterial growth is not fully understood but it has been found to cause inhibition of protein synthesis and DNA gyrase activity in vitro.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 217.04 g/mol
• Formel: C₈H₆BrFO
• Reinheit: Min. 95%
• Farbe/Form: White To Yellow To Brown Solid
• InChl: InChI=1S/C8H6BrFO/c9-5-8(11)6-1-3-7(10)4-2-6/h1-4H,5H2
• InChI Key: InChIKey=ZJFWCELATJMDNO-UHFFFAOYSA-N
• SMILES: O=C(CBr)c1ccc(F)cc1