tert-Butyl (5-hydroxy-2-methylpentan-2-yl)carbamate

≥95%

Reagent Code: #82907
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CAS Number 1123693-87-7

science Other reagents with same CAS 1123693-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.31 g/mol
Formula C₁₁H₂₃NO₃
badge Registry Numbers
MDL Number MFCD24467554
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound, tert-Butyl (5-hydroxy-2-methylpentan-2-yl)carbamate, is a specialized organic intermediate featuring a tert-butoxycarbonyl (Boc) protected amine and a free hydroxyl group. It is primarily used in pharmaceutical synthesis as a building block for complex molecules, where the Boc group protects the amine during selective functionalization of the hydroxyl or other reactions. Its structure allows for stepwise deprotection and coupling in the production of active pharmaceutical ingredients (APIs) and peptide analogs. The stability of the Boc protection under acidic and basic conditions makes it valuable in multi-step organic transformations for drug discovery and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,350.00

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tert-Butyl (5-hydroxy-2-methylpentan-2-yl)carbamate
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This compound, tert-Butyl (5-hydroxy-2-methylpentan-2-yl)carbamate, is a specialized organic intermediate featuring a tert-butoxycarbonyl (Boc) protected amine and a free hydroxyl group. It is primarily used in pharmaceutical synthesis as a building block for complex molecules, where the Boc group protects the amine during selective functionalization of the hydroxyl or other reactions. Its structure allows for stepwise deprotection and coupling in the production of active pharmaceutical ingredients (APIs

This compound, tert-Butyl (5-hydroxy-2-methylpentan-2-yl)carbamate, is a specialized organic intermediate featuring a tert-butoxycarbonyl (Boc) protected amine and a free hydroxyl group. It is primarily used in pharmaceutical synthesis as a building block for complex molecules, where the Boc group protects the amine during selective functionalization of the hydroxyl or other reactions. Its structure allows for stepwise deprotection and coupling in the production of active pharmaceutical ingredients (APIs) and peptide analogs. The stability of the Boc protection under acidic and basic conditions makes it valuable in multi-step organic transformations for drug discovery and medicinal chemistry.

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