6-Iodo-4-methylquinoline

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Reagent Code: #200289
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CAS Number 57830-59-8

science Other reagents with same CAS 57830-59-8

blur_circular Chemical Specifications

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Weight 269.08 g/mol
Formula C₁₀H₈IN
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies, especially in oncology research. The iodo group facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of complex aromatic or heteroaromatic systems. It is also employed in the preparation of fluorescent probes and imaging agents due to the inherent photophysical properties of the quinoline core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,540.00
inventory 250mg
10-20 days ฿5,480.00
inventory 1g
10-20 days ฿20,290.00

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6-Iodo-4-methylquinoline
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies, especially in oncology research. The iodo group facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of complex aromatic or heteroaromatic systems. It is also employed in t

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies, especially in oncology research. The iodo group facilitates cross-coupling reactions such as Suzuki or Heck reactions, enabling the introduction of complex aromatic or heteroaromatic systems. It is also employed in the preparation of fluorescent probes and imaging agents due to the inherent photophysical properties of the quinoline core.

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