tert-Butyl 4-aminoisoindoline-2-carboxylate

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Reagent Code: #146422
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CAS Number 871013-98-8

science Other reagents with same CAS 871013-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.29 g/mol
Formula C₁₃H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD10566550
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting cancer and inflammatory diseases. The tert-butyl ester serves as a protecting group for the carboxylate, facilitating selective reactions at the free amino group and enabling efficient multi-step synthesis. Commonly employed in medicinal chemistry for lead optimization due to its stability and compatibility with various coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿1,040.00
100mg
10-20 days ฿2,500.00
250mg
10-20 days ฿4,440.00
5g
10-20 days ฿77,190.00
1g
10-20 days ฿15,440.00

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tert-Butyl 4-aminoisoindoline-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting cancer and inflammatory diseases. The tert-butyl ester serves as a protecting group for the carboxylate, facilitating selective reactions at the free amino group and enabling efficient multi-step synthesis. Commonly employed in medicinal chemistry
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of complex heterocyclic systems found in drug candidates targeting cancer and inflammatory diseases. The tert-butyl ester serves as a protecting group for the carboxylate, facilitating selective reactions at the free amino group and enabling efficient multi-step synthesis. Commonly employed in medicinal chemistry for lead optimization due to its stability and compatibility with various coupling reactions.
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