4-Iodo-N-methylbenzamide

98%

Reagent Code: #200482
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CAS Number 89976-43-2

science Other reagents with same CAS 89976-43-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.06 g/mol
Formula C₈H₈INO
badge Registry Numbers
MDL Number MFCD02945450
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure allows for facile modification through cross-coupling reactions, making it valuable in the development of new bioactive compounds. Commonly employed in the preparation of substituted aromatic compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the synthesis of potential receptor ligands and enzyme inhibitors due to the presence of both amide and iodo functionalities, which can engage in hydrogen bonding and metal coordination.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿680.00
inventory 1g
10-20 days ฿1,650.00
inventory 5g
10-20 days ฿7,510.00
inventory 10g
10-20 days ฿13,600.00
inventory 25g
10-20 days ฿32,360.00

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4-Iodo-N-methylbenzamide
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Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure allows for facile modification through cross-coupling reactions, making it valuable in the development of new bioactive compounds. Commonly employed in the preparation of substituted aromatic compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the synthesis of potential receptor ligands and enzyme inhibitors due to the presence of both

Used primarily as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure allows for facile modification through cross-coupling reactions, making it valuable in the development of new bioactive compounds. Commonly employed in the preparation of substituted aromatic compounds via palladium-catalyzed reactions such as Suzuki or Heck couplings. Also utilized in the synthesis of potential receptor ligands and enzyme inhibitors due to the presence of both amide and iodo functionalities, which can engage in hydrogen bonding and metal coordination.

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