N-Cyclopropyl-4-iodobenzamide

98%

Reagent Code: #215753
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CAS Number 794539-14-3

science Other reagents with same CAS 794539-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.1 g/mol
Formula C₁₀H₁₀INO
badge Registry Numbers
MDL Number MFCD04685309
thermostat Physical Properties
Boiling Point 389.9±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.77±0.1 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. The iodobenzene moiety allows for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropyl group contributes metabolic stability and can influence binding affinity in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid framework and halogen handle for further functionalization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿3,590.00
inventory 1g
10-20 days ฿9,700.00

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N-Cyclopropyl-4-iodobenzamide
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Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. The iodobenzene moiety allows for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropyl group contributes metabolic stability and can influence binding affinity in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigi

Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. The iodobenzene moiety allows for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The cyclopropyl group contributes metabolic stability and can influence binding affinity in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid framework and halogen handle for further functionalization.

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