tert-Butyl 4-hydroxyisoindoline-2-carboxylate

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Reagent Code: #152329
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CAS Number 871013-92-2

science Other reagents with same CAS 871013-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.28 g/mol
Formula C₁₃H₁₇NO₃
badge Registry Numbers
MDL Number MFCD10700131
thermostat Physical Properties
Boiling Point 359.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.205±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of isoindoline-based scaffolds, which are found in compounds with potential neuroprotective, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for derivatization and ring modification to enhance drug potency and metabolic stability. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its favorable functional group compatibility and stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿780.00
inventory 250mg
10-20 days ฿1,920.00

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tert-Butyl 4-hydroxyisoindoline-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of isoindoline-based scaffolds, which are found in compounds with potential neuroprotective, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for derivatization and ring modification to enhance drug potency and metabolic stability. Also utilized in

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure supports the construction of isoindoline-based scaffolds, which are found in compounds with potential neuroprotective, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for derivatization and ring modification to enhance drug potency and metabolic stability. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its favorable functional group compatibility and stability.

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