N-(4-Iodophenyl)cyclopropanecarboxamide

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Reagent Code: #218928
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CAS Number 23779-17-1

science Other reagents with same CAS 23779-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.10 g/mol
Formula C₁₀H₁₀INO
badge Registry Numbers
MDL Number MFCD01327898
thermostat Physical Properties
Melting Point 214-216 °C
Boiling Point 411.5±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.865±0.06 g/cm3(Predicted)
Storage 2-8°C, store away from light, dry seal

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropanecarboxamide moiety contributes rigidity and metabolic stability, making it valuable in medicinal chemistry for designing enzyme inhibitors or receptor ligands. Commonly employed in the development of radiolabeled compounds for imaging studies due to the presence of iodine. Also serves as a building block in the synthesis of functionalized amides for drug discovery research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿700.00
inventory 5g
10-20 days ฿3,360.00
inventory 10g
10-20 days ฿6,180.00

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N-(4-Iodophenyl)cyclopropanecarboxamide
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropanecarboxamide moiety contributes rigidity and metabolic stability, making it valuable in medicinal chemistry for designing enzyme inhibitors or receptor ligands. Commonly employed in the development of radiolabeled compounds for imaging studies due to the

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropanecarboxamide moiety contributes rigidity and metabolic stability, making it valuable in medicinal chemistry for designing enzyme inhibitors or receptor ligands. Commonly employed in the development of radiolabeled compounds for imaging studies due to the presence of iodine. Also serves as a building block in the synthesis of functionalized amides for drug discovery research.

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