tert-butyl but-3-enyl(methyl)carbamate

≥95%

Reagent Code: #238594
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CAS Number 312728-28-2

science Other reagents with same CAS 312728-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.2634 g/mol
Formula C₁₀H₁₉NO₂
badge Registry Numbers
MDL Number MFCD21648472
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 agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling controlled deprotection without affecting other functional groups. Additionally, the presence of the butenyl chain offers a site for further chemical modifications, such as cross-coupling reactions or cyclizations, useful in building complex molecular frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿8,000.00
inventory 1g
10-20 days ฿24,000.00
tert-butyl but-3-enyl(methyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling controlled deprotection without affecting other functional groups. Additionally, the presence of the butenyl chain off

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients. The tert-butyl carbamate group can be easily removed under mild acidic conditions, enabling controlled deprotection without affecting other functional groups. Additionally, the presence of the butenyl chain offers a site for further chemical modifications, such as cross-coupling reactions or cyclizations, useful in building complex molecular frameworks.

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