Ethyl (E)-3-(4-bromophenyl)prop-2-enoate

CAS: 24393-53-1

Ref. 3D-ZAA39353

Produktinformation

• Name: Ethyl (E)-3-(4-bromophenyl)prop-2-enoate
• Synonyme: (E)-3-(4-Bromophenyl)-2-propenoic acid ethyl ester, (E)-3-(4-Bromophenyl)acrylic acid ethyl ester, (E)-Ethyl 3-(4-bromophenyl)acrylate, 2-Propenoic acid, 3-(4-bromophenyl)-, ethyl ester, 2-Propenoic acid, 3-(4-bromophenyl)-, ethyl ester, (2E)-, 2-Propenoic acid, 3-(4-bromophenyl)-, ethyl ester, (E)-, Cinnamic acid, p-bromo-, ethyl ester, (E)-, Ethyl (2E)-3-(4-bromophenyl)-2-propenoate, Ethyl (E)-3-(4-Bromophenyl)acrylate, Ethyl (E)-3-(4-bromophenyl)-2-propenoate, Ethyl (E)-4-bromocinnamate, Ethyl 3-(4-Bromophenyl)Prop-2-Enoate, Nsc 636702, ethyl (2E)-3-(4-bromophenyl)prop-2-enoate, trans-p-Bromocinnamic acid ethyl ester

Beschreibung

Ethyl (E)-3-(4-bromophenyl)prop-2-enoate is a versatile compound with various biological effects. It has an acidic nature and can interact with glycine, fatty acids, caffeine, gamma-aminobutyric acid, 14-hydroxycodeinone, glycerin, and ion extraction. This compound is commonly used in the research field as a tool for studying oral opioids and adenosine receptor antagonists.

With its polyene structure, Ethyl (E)-3-(4-bromophenyl)prop-2-enoate exhibits unique properties that make it suitable for different applications. It has been found to have monoamine-like activity, which can potentially impact neurotransmitter systems in the body. Additionally, this compound has shown promising results in studies involving breast cancer cells (MCF-7), indicating its potential as an anti-cancer agent.

Overall, Ethyl (E)-3-(4-bromophenyl)

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 255.11 g/mol
• Formel: C₁₁H₁₁BrO₂
• Reinheit: Min. 95%