tert-Butyl diallylcarbamate

98%,stabilized with 200ppm MEHQ

Reagent Code: #140740
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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 75 °C at 1.5 mmHg
inventory_2 Storage & Handling
Density 0.914 g/mL at 25 °C (lit.)
Storage 2-8°C, sealed, inert gas storage

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a protected form of diallylamine, enabling selective reactions in multi-step syntheses without interference from the amine group. Commonly employed in pharmaceutical manufacturing where controlled nitrogen incorporation is required. Also utilized in polymer chemistry to introduce allyl functionalities that can undergo further cross-linking or modification reactions. Its stability under various reaction conditions makes it valuable in industrial and laboratory-scale processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿440.00
inventory 25g
10-20 days ฿1,460.00
inventory 100g
10-20 days ฿5,490.00
inventory 500g
10-20 days ฿20,070.00

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tert-Butyl diallylcarbamate
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Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a protected form of diallylamine, enabling selective reactions in multi-step syntheses without interference from the amine group. Commonly employed in pharmaceutical manufacturing where controlled nitrogen incorporation is required. Also utilized in polymer chemistry to introduce allyl functionalities that can undergo further cross-linking or modification reac

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a protected form of diallylamine, enabling selective reactions in multi-step syntheses without interference from the amine group. Commonly employed in pharmaceutical manufacturing where controlled nitrogen incorporation is required. Also utilized in polymer chemistry to introduce allyl functionalities that can undergo further cross-linking or modification reactions. Its stability under various reaction conditions makes it valuable in industrial and laboratory-scale processes.

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