tert-Butyl 5-bromo-4-fluoroindoline-1-carboxylate

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Reagent Code: #148760
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CAS Number 1337533-31-9

science Other reagents with same CAS 1337533-31-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.17 g/mol
Formula C₁₃H₁₅BrFNO₂
badge Registry Numbers
MDL Number MFCD29760339
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used 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 constructing complex indoline-based molecules. Commonly employed in medicinal chemistry for SAR studies due to the bromo and fluoro substituents, which serve as handles for cross-coupling reactions and influence bioavailability. Also utilized in the preparation of serotonin receptor modulators and other bioactive agents targeting neurological disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,040.00
inventory 1g
10-20 days ฿39,480.00
inventory 5g
10-20 days ฿153,300.00

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tert-Butyl 5-bromo-4-fluoroindoline-1-carboxylate
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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. Its structure allows for selective functionalization, making it valuable in constructing complex indoline-based molecules. Commonly employed in medicinal chemistry for SAR studies due to the bromo and fluoro substituents, which serve as handles for cross-coupling reactions and influence bioavailability. Also utilized in the preparation of serotonin receptor m

Used 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 constructing complex indoline-based molecules. Commonly employed in medicinal chemistry for SAR studies due to the bromo and fluoro substituents, which serve as handles for cross-coupling reactions and influence bioavailability. Also utilized in the preparation of serotonin receptor modulators and other bioactive agents targeting neurological disorders.

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