4-Chloro-5-fluoroindoline-2,3-dione

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Reagent Code: #162140
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CAS Number 84378-94-9

science Other reagents with same CAS 84378-94-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.57 g/mol
Formula C₈H₃ClFNO₂
badge Registry Numbers
MDL Number MFCD03618550
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its ability to undergo specific derivatization reactions, useful in biochemical imaging and assay development. Additionally, it serves as a building block in the design of novel heterocyclic compounds for drug discovery research.

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Test Parameter Specification
Appearance White to yellow to orange powder or crystals
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 5g
10-20 days ฿5,880.00
inventory 250mg
10-20 days ฿258.00

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4-Chloro-5-fluoroindoline-2,3-dione
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its ability to undergo specific derivatization reactions, useful in biochemical imaging and assay development. Additionally, it ser

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. It is also employed in the preparation of fluorescent probes due to its ability to undergo specific derivatization reactions, useful in biochemical imaging and assay development. Additionally, it serves as a building block in the design of novel heterocyclic compounds for drug discovery research.

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