tert-Butyl diallylcarbamate

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Reagent Code: #145071
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CAS Number 151259-38-0

science Other reagents with same CAS 151259-38-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.27 g/mol
Formula C₁₁H₁₉NO₂
thermostat Physical Properties
Boiling Point 242.7°C
inventory_2 Storage & Handling
Density 0.914 g/mL at 25 °C (lit.)
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing compounds. It serves as a protected amine reagent in multi-step synthesis, offering stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in pharmaceutical manufacturing for building complex amine architectures, especially in protease inhibitors and other bioactive molecules. Its allyl groups enable further functionalization via cross-coupling or olefin transformation reactions, making it valuable in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 10g
10-20 days ฿780.00
inventory 250g
10-20 days ฿10,880.00
inventory 50g
10-20 days ฿2,350.00

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tert-Butyl diallylcarbamate
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Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing compounds. It serves as a protected amine reagent in multi-step synthesis, offering stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in pharmaceutical manufacturing for building complex amine architectures, especially in protease inhibitors and other bioactive molecules. Its allyl groups enable further functionalization via cross-coupling

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing compounds. It serves as a protected amine reagent in multi-step synthesis, offering stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in pharmaceutical manufacturing for building complex amine architectures, especially in protease inhibitors and other bioactive molecules. Its allyl groups enable further functionalization via cross-coupling or olefin transformation reactions, making it valuable in medicinal chemistry and process development.

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