1-tert-Butyl 6-methyl indoline-1,6-dicarboxylate

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Reagent Code: #150430
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CAS Number 1220039-51-9

science Other reagents with same CAS 1220039-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.32 g/mol
Formula C₁₅H₁₉NO₄
badge Registry Numbers
MDL Number MFCD09878912
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems, such as indolines. Commonly employed in research settings to design compounds targeting neurological disorders and inflammatory conditions. The tert-butyl ester group provides stability, aiding in protective strategies during synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿2,470.00
inventory 1g
10-20 days ฿5,880.00
inventory 5g
10-20 days ฿29,350.00

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1-tert-Butyl 6-methyl indoline-1,6-dicarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems, such as indolines. Commonly employed in research settings to design compounds targeting neurological disorders and inflammatory conditions. The tert-butyl ester group provides stability, aiding in protective strategies

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems, such as indolines. Commonly employed in research settings to design compounds targeting neurological disorders and inflammatory conditions. The tert-butyl ester group provides stability, aiding in protective strategies during synthesis.

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