N-(4-Iodophenyl)benzamide

95%

Reagent Code: #219183
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CAS Number 52807-29-1

science Other reagents with same CAS 52807-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.13 g/mol
Formula C₁₃H₁₀INO
badge Registry Numbers
MDL Number MFCD00447600
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its structure supports cross-coupling reactions, making it valuable in the preparation of biaryl compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. The iodine substituent acts as a reactive handle for further functionalization, enabling the construction of complex aromatic systems. It is also employed in the development of bioactive molecules, including potential anti-inflammatory or antimicrobial agents, due to the presence of both amide and aryl iodide functionalities that can interact with biological targets. Additionally, it finds use in materials science for designing aromatic frameworks with specific electronic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,240.00
inventory 5g
10-20 days ฿4,220.00
inventory 25g
10-20 days ฿14,760.00

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N-(4-Iodophenyl)benzamide
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Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its structure supports cross-coupling reactions, making it valuable in the preparation of biaryl compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. The iodine substituent acts as a reactive handle for further functionalization, enabling the construction of complex aromatic systems. It is also employed in the development of bioactive molecules, including potential an

Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its structure supports cross-coupling reactions, making it valuable in the preparation of biaryl compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. The iodine substituent acts as a reactive handle for further functionalization, enabling the construction of complex aromatic systems. It is also employed in the development of bioactive molecules, including potential anti-inflammatory or antimicrobial agents, due to the presence of both amide and aryl iodide functionalities that can interact with biological targets. Additionally, it finds use in materials science for designing aromatic frameworks with specific electronic properties.

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