2-(tert-butoxycarbonyl)isoindoline-4-carboxylicacid

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Reagent Code: #244412
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CAS Number 1044764-69-3

science Other reagents with same CAS 1044764-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
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MDL Number MFCD10700129
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected nitrogen functionalities. The Boc-protected isoindoline core is also utilized in the preparation of proteolysis targeting chimeras (PROTACs) and other targeted degradation agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,210.00
inventory 1g
10-20 days ฿60,520.00
inventory 250mg
10-20 days ฿17,400.00
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2-(tert-butoxycarbonyl)isoindoline-4-carboxylicacid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected nitrogen functionalities. The Boc-protected isoindoline core is also utilized in th

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected nitrogen functionalities. The Boc-protected isoindoline core is also utilized in the preparation of proteolysis targeting chimeras (PROTACs) and other targeted degradation agents.

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