4-Chloroindolin-2-one

98%

Reagent Code: #160261
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CAS Number 20870-77-3

science Other reagents with same CAS 20870-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.59 g/mol
Formula C₈H₆ClNO
thermostat Physical Properties
Melting Point 206-208°C
Boiling Point 340.3°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive indole derivatives. Also employed in the preparation of functionalized oxindoles, which show activity in neurological and anti-inflammatory applications. Its chloro-substituent allows for further functionalization via cross-coupling reactions, making it valuable in drug discovery and organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿340.00
inventory 1g
10-20 days ฿710.00
4-Chloroindolin-2-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive indole derivatives. Also employed in the preparation of functionalized oxindoles, which show activity in neurological and anti-inflammatory applications. Its chloro-substituent allows for further functionalization via cross-coupling reactions, making it valuable in drug

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive indole derivatives. Also employed in the preparation of functionalized oxindoles, which show activity in neurological and anti-inflammatory applications. Its chloro-substituent allows for further functionalization via cross-coupling reactions, making it valuable in drug discovery and organic synthesis.

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