5-Iodoquinoline

98%

Reagent Code: #201148
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CAS Number 1006-50-4

science Other reagents with same CAS 1006-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.05 g/mol
Formula C₉H₆NI
badge Registry Numbers
MDL Number MFCD11183301
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and iodine functionality. The iodine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. Employed in research settings to develop fluorescent probes and sensors owing to the quinoline ring’s photophysical properties. Also investigated for its antimicrobial activity and potential use in medicinal chemistry for targeting DNA in cancer cells.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,690.00
inventory 250mg
10-20 days ฿2,780.00
inventory 1g
10-20 days ฿5,570.00
inventory 5g
10-20 days ฿19,320.00
5-Iodoquinoline
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and iodine functionality. The iodine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. Employed in research settings to develop fluorescent probes and sensors owing to the quinoline ring’s photophysical properties. Also investigated for its antimicrobial

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and iodine functionality. The iodine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions. Employed in research settings to develop fluorescent probes and sensors owing to the quinoline ring’s photophysical properties. Also investigated for its antimicrobial activity and potential use in medicinal chemistry for targeting DNA in cancer cells.

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