2-Bromo-4'-methoxy acetophenone

CAS: 2632-13-5

Ref. 3D-FB46009

Produktinformation

• Name: 2-Bromo-4'-methoxy acetophenone
• Synonyme: 1-(Bromoacetyl)-4-methoxybenzene, 2-(4-Methoxyphenyl)-2-oxoethyl bromide, 2-Bromo-(4-methoxyphenyl)ethan-1-one, 2-Bromo-1-(4-Methoxyphenyl)Ethanone, 2-Bromo-1-(4-methoxyphenyl)-1-ethanone, 2-Bromo-1-(4-methoxyphenyl)ethan-1-one, 2-Bromo-1-[4-(methyloxy)phenyl]ethanone, 2-Bromo-4-Methoxy Acetophenone, 2-Bromo-4-Methoxyacetophenone, 2-Bromo-p-methoxyacetophenone, 4'-Methoxy-2-bromoacetophenone, 4-(Bromoacetyl)Anisole, 4-Methoxy Phenecyl Bromide, 4-Methoxy-a-brommoacetophjenone, 4-Methoxyphenacyl Br, 4-Methoxyphenacyl bromide, A-Bromo-P-Methoxyacetophenone, Acetophenone, 2-Bromo-4'-Methoxy-, Alpha-Bromo-4-methoxyacetophenone, Brommethyl-4-methoxyphenylketon, Bromomethyl 4-methoxyphenyl ketone, Bromomethyl p-anisyl ketone, Bromomethyl p-methoxyphenyl ketone, Bromomethyl-4-methoxyphenylcetone, Bromometil-4-Metoxifenilcetona, Ethanone, 2-bromo-1-(4-methoxyphenyl)-, Nsc 129010, PTP Inhibitor II, p-Methoxy-2-bromoacetophenone, p-Methoxyphenacyl bromide, Α-Bromo-Paramethoxylacetophenone, ω-Bromo-4'-methoxyacetophenone, ω-Bromo-p-methoxyacetophenone

Beschreibung

2-Bromo-4'-methoxy acetophenone (2-BMA) is a reactive chemical that is used in the synthesis of organic compounds. It has been shown to induce neuronal death by causing an increase in intracellular calcium concentration and a decrease in extracellular potassium concentration. 2-BMA also inhibits phosphatases, which are enzymes that break down phosphoric esters, leading to an accumulation of these molecules, which can lead to cancer. 2-BMA binds to monoclonal antibodies and prevents their ability to bind with antigens on cells. This binding leads to reduced immune response and increased risk for HIV infection. 2-BMA can be synthesized by reacting bromine with 4'-methoxyacetophenone or 4'-hydroxyacetophenone under acidic conditions. The molecular geometry of the molecule is linear and its reactivity is due to the presence of a carbonyl group. The chemical shifts observed in 2-

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 229.07 g/mol
• Formel: C₉H₉BrO₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C9H9BrO2/c1-12-8-4-2-7(3-5-8)9(11)6-10/h2-5H,6H2,1H3
• InChI Key: InChIKey=XQJAHBHCLXUGEP-UHFFFAOYSA-N
• SMILES: COc1ccc(C(=O)CBr)cc1