3-Bromo-N-cyclopentylbenzamide

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Reagent Code: #154547
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CAS Number 349405-34-1

science Other reagents with same CAS 349405-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.15 g/mol
Formula C₁₂H₁₄BrNO
badge Registry Numbers
MDL Number MFCD00751460
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical research. It serves as a building block for developing bioactive molecules due to the presence of both amide and bromo functionalities, which allow for further chemical modifications. The bromine atom enables cross-coupling reactions such as Suzuki or Heck reactions, facilitating the construction of complex aromatic systems. The amide group can engage in hydrogen bonding, making it useful in the design of enzyme inhibitors or receptor ligands. Commonly employed in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in the synthesis of cyclopentyl-containing analogs for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,240.00
inventory 5g
10-20 days ฿23,080.00

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3-Bromo-N-cyclopentylbenzamide
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Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical research. It serves as a building block for developing bioactive molecules due to the presence of both amide and bromo functionalities, which allow for further chemical modifications. The bromine atom enables cross-coupling reactions such as Suzuki or Heck reactions, facilitating the construction of complex aromatic systems. The amide group can engage in hydrogen bonding, making it useful in the design of enzyme inhibi

Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical research. It serves as a building block for developing bioactive molecules due to the presence of both amide and bromo functionalities, which allow for further chemical modifications. The bromine atom enables cross-coupling reactions such as Suzuki or Heck reactions, facilitating the construction of complex aromatic systems. The amide group can engage in hydrogen bonding, making it useful in the design of enzyme inhibitors or receptor ligands. Commonly employed in the development of central nervous system agents and anti-inflammatory compounds. Also utilized in the synthesis of cyclopentyl-containing analogs for structure-activity relationship (SAR) studies.

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