(2E)-N-(4-Bromophenyl)-3-ethoxy-2-propenamide

99%

Reagent Code: #36460
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CAS Number 327058-51-5

science Other reagents with same CAS 327058-51-5

blur_circular Chemical Specifications

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Weight 270.12 g/mol
Formula C₁₁H₁₂BrNO₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

(2E)-N-(4-Bromophenyl)-3-ethoxy-2-propenamide is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting inflammation and cancer. The presence of the bromophenyl group enhances its reactivity, making it valuable for cross-coupling reactions in medicinal chemistry. Additionally, its ethoxy and propenamide functionalities contribute to its role in designing molecules with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Researchers also explore its use in material science for creating advanced polymers with specific electronic or optical properties.

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Test Parameter Specification
Purity 98.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿33,460.00

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(2E)-N-(4-Bromophenyl)-3-ethoxy-2-propenamide
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(2E)-N-(4-Bromophenyl)-3-ethoxy-2-propenamide is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting inflammation and cancer. The presence of the bromophenyl group enhances its reactivity, making it valuable for cross-coupling reactions in medicinal chemistry. Additionally, its ethoxy and propenamide functionalities contribute to its role in designing molecules with potential t

(2E)-N-(4-Bromophenyl)-3-ethoxy-2-propenamide is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting inflammation and cancer. The presence of the bromophenyl group enhances its reactivity, making it valuable for cross-coupling reactions in medicinal chemistry. Additionally, its ethoxy and propenamide functionalities contribute to its role in designing molecules with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Researchers also explore its use in material science for creating advanced polymers with specific electronic or optical properties.

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