tert-Butyl (1-hydroxy-4-methylpentan-2-yl)carbamate

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Reagent Code: #61072
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CAS Number 142121-48-0

science Other reagents with same CAS 142121-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.31 g/mol
Formula C₁₁H₂₃NO₃
thermostat Physical Properties
Boiling Point 319.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound, tert-Butyl (1-hydroxy-4-methylpentan-2-yl)carbamate, is a protected amino alcohol intermediate featuring a tert-butoxycarbonyl (Boc) group on the amine and a free hydroxyl group. It is primarily used in organic synthesis, particularly for peptides and pharmaceuticals, where the Boc protection allows selective manipulation of the hydroxyl functionality in multi-step reactions. The protecting group can be readily removed under acidic conditions, making it essential for constructing complex molecules in active pharmaceutical ingredient (API) production and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,816.00
inventory 250mg
10-20 days ฿1,575.00

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tert-Butyl (1-hydroxy-4-methylpentan-2-yl)carbamate
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This compound, tert-Butyl (1-hydroxy-4-methylpentan-2-yl)carbamate, is a protected amino alcohol intermediate featuring a tert-butoxycarbonyl (Boc) group on the amine and a free hydroxyl group. It is primarily used in organic synthesis, particularly for peptides and pharmaceuticals, where the Boc protection allows selective manipulation of the hydroxyl functionality in multi-step reactions. The protecting group can be readily removed under acidic conditions, making it essential for constructing complex mole
This compound, tert-Butyl (1-hydroxy-4-methylpentan-2-yl)carbamate, is a protected amino alcohol intermediate featuring a tert-butoxycarbonyl (Boc) group on the amine and a free hydroxyl group. It is primarily used in organic synthesis, particularly for peptides and pharmaceuticals, where the Boc protection allows selective manipulation of the hydroxyl functionality in multi-step reactions. The protecting group can be readily removed under acidic conditions, making it essential for constructing complex molecules in active pharmaceutical ingredient (API) production and medicinal chemistry research.
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