tert-Butyl (4-hydroxybutan-2-yl)carbamate

95%

Reagent Code: #145299
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CAS Number 146514-31-0

science Other reagents with same CAS 146514-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.25 g/mol
Formula C₉H₁₉NO₃
thermostat Physical Properties
Boiling Point 301.4±25.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in constructing complex molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where protection of amine groups is required during multi-step reactions. The tert-butyl carbamate moiety acts as a protecting group that can be removed under mild acidic conditions, enabling controlled deprotection in peptide and heterocyclic synthesis. Also utilized in the production of agrochemicals and specialty polymers due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿3,000.00
inventory 5g
10-20 days ฿14,300.00
inventory 10g
10-20 days ฿28,570.00
inventory 25g
10-20 days ฿62,100.00

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tert-Butyl (4-hydroxybutan-2-yl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in constructing complex molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where protection of amine groups is required during multi-step reactions. The tert-butyl carbamate moiety acts as a protecting group that can be removed under mild acidic condit

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in constructing complex molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) where protection of amine groups is required during multi-step reactions. The tert-butyl carbamate moiety acts as a protecting group that can be removed under mild acidic conditions, enabling controlled deprotection in peptide and heterocyclic synthesis. Also utilized in the production of agrochemicals and specialty polymers due to its stability and reactivity profile.

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