6-Iodoindolin-2-one

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Reagent Code: #200583
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CAS Number 919103-45-0

science Other reagents with same CAS 919103-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₈H₆INO
badge Registry Numbers
MDL Number MFCD09835633
thermostat Physical Properties
Boiling Point 365 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the iodine moiety, enabling cross-coupling reactions such as Suzuki or Heck reactions to introduce diverse aromatic or heteroaromatic groups. Its indolinone core is commonly found in bioactive molecules, making it valuable in drug discovery programs targeting tyrosine kinase pathways. Also explored in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the heavy atom effect of iodine, which can influence photophysical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,780.00
inventory 250mg
10-20 days ฿2,690.00
inventory 5g
10-20 days ฿31,190.00
inventory 1g
10-20 days ฿7,840.00

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6-Iodoindolin-2-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the iodine moiety, enabling cross-coupling reactions such as Suzuki or Heck reactions to introduce diverse aromatic or heteroaromatic groups. Its indolinone core is commonly found in bioactive molecules, making it valuable in drug discovery programs targeting tyrosine kinase pathway

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to the reactivity of the iodine moiety, enabling cross-coupling reactions such as Suzuki or Heck reactions to introduce diverse aromatic or heteroaromatic groups. Its indolinone core is commonly found in bioactive molecules, making it valuable in drug discovery programs targeting tyrosine kinase pathways. Also explored in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the heavy atom effect of iodine, which can influence photophysical properties.

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