CAS 51149-28-1

Ethanone, 2-bromo-1-(4-hydroxy-3,5-dimethoxyphenyl)-

Description:

Ethanone, 2-bromo-1-(4-hydroxy-3,5-dimethoxyphenyl)-, also known by its CAS number 51149-28-1, is an organic compound characterized by its functional groups and structural features. It contains a bromine atom, which contributes to its reactivity, and a phenolic hydroxyl group that can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of methoxy groups (–OCH3) on the aromatic ring increases the electron density, influencing its chemical behavior and potential biological activity. This compound is typically synthesized through bromination and subsequent reactions involving phenolic compounds. Its structure suggests potential applications in pharmaceuticals or as an intermediate in organic synthesis, particularly in the development of compounds with biological activity. The specific arrangement of substituents on the aromatic ring can significantly affect its properties, including its reactivity, stability, and interaction with biological systems. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.

Formula: C₁₀H₁₁BrO₄

α-Bromoacetosyringone

Controlled Product

CAS: 51149-28-1

Formula: C₁₀H₁₁BrO₄

Color and Shape: Neat

Molecular weight: 275.1

Ref: TR-B679350

α-Bromoacetosyringone

CAS: 51149-28-1

α-Bromoacetosyringone is a research tool that can be used as an activator, ligand or receptor. It has been shown to have a high affinity for antibody and ion channels. α-Bromoacetosyringone also has the ability to bind to and inhibit protein interactions.

Formula: C₁₀H₁₁BrO₄

Purity: Min. 95%

Molecular weight: 275.1 g/mol

Ref: 3D-BCA14928