N-(4-Iodophenyl)-4-(morpholinomethyl)benzamide

98%

Reagent Code: #215779
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CAS Number 333357-56-5

science Other reagents with same CAS 333357-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 422.26 g/mol
Formula C₁₈H₁₉IN₂O₂
thermostat Physical Properties
Boiling Point 435.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.576±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of bioactive molecules and receptor ligands. Its structure supports conjugation in medicinal chemistry, making it valuable in creating potential anticancer and anti-inflammatory agents. Commonly utilized in Suzuki and other cross-coupling reactions due to the iodine moiety, enabling the formation of biaryl derivatives. Also serves as a building block in the synthesis of kinase inhibitors and CNS-targeted drugs owing to the morpholine ring’s favorable pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿12,180.00
inventory 25mg
10-20 days ฿24,340.00
inventory 50mg
10-20 days ฿41,360.00
inventory 100mg
10-20 days ฿70,310.00
inventory 250mg
10-20 days ฿119,490.00

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N-(4-Iodophenyl)-4-(morpholinomethyl)benzamide
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Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of bioactive molecules and receptor ligands. Its structure supports conjugation in medicinal chemistry, making it valuable in creating potential anticancer and anti-inflammatory agents. Commonly utilized in Suzuki and other cross-coupling reactions due to the iodine moiety, enabling the formation of biaryl derivatives. Also serves as a building block in the synthesis of kinase inhibitors and CNS-tar

Used in organic synthesis as an intermediate for pharmaceutical compounds, particularly in the development of bioactive molecules and receptor ligands. Its structure supports conjugation in medicinal chemistry, making it valuable in creating potential anticancer and anti-inflammatory agents. Commonly utilized in Suzuki and other cross-coupling reactions due to the iodine moiety, enabling the formation of biaryl derivatives. Also serves as a building block in the synthesis of kinase inhibitors and CNS-targeted drugs owing to the morpholine ring’s favorable pharmacokinetic properties.

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