4-(4-Iodophenoxymethyl)pyridine

95%

Reagent Code: #200644
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CAS Number 944278-91-5

science Other reagents with same CAS 944278-91-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.12 g/mol
Formula C₁₂H₁₀INO
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MDL Number MFCD14648758
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic systems in drug design. Also utilized in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine, enabling applications in PET or SPECT imaging.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,100.00
inventory 1g
10-20 days ฿32,560.00

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4-(4-Iodophenoxymethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic systems in drug design. Also utilized in the preparation of radiolabeled compounds for imaging studi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic or heteroaromatic systems in drug design. Also utilized in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine, enabling applications in PET or SPECT imaging.

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