5-Iodoindolin-2-one

95%

Reagent Code: #200483
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CAS Number 193354-13-1

science Other reagents with same CAS 193354-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₈H₆INO
badge Registry Numbers
MDL Number MFCD08669500
thermostat Physical Properties
Boiling Point 382.8±42.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, avoid light, and inert gas storage

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential anticancer, antiviral, and antimicrobial activities. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the reactive iodine moiety. Also utilized in medicinal chemistry for the development of kinase inhibitors and neuroprotective agents. Its structure allows easy functionalization at multiple positions, making it valuable in drug discovery research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿630.00
inventory 250mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿3,100.00
inventory 5g
10-20 days ฿11,570.00
inventory 25g
10-20 days ฿47,080.00

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5-Iodoindolin-2-one
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential anticancer, antiviral, and antimicrobial activities. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the reactive iodine moiety. Also utilized in medicinal chemistry for the development of kinase inhibitors and neuroprotective agents. Its structure allows easy functionalization at multipl

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the preparation of indole-based derivatives with potential anticancer, antiviral, and antimicrobial activities. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the reactive iodine moiety. Also utilized in medicinal chemistry for the development of kinase inhibitors and neuroprotective agents. Its structure allows easy functionalization at multiple positions, making it valuable in drug discovery research.

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