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

97%

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.

Available Sizes & Pricing

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

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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