tert-Butyl (1-bromopropan-2-yl)carbamate

97%

Reagent Code: #148610
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CAS Number 1391026-59-7

science Other reagents with same CAS 1391026-59-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.12 g/mol
Formula C₈H₁₆BrNO₂
badge Registry Numbers
MDL Number MFCD24167884
inventory_2 Storage & Handling
Storage -20°C, dry seal

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It serves as a protected amine derivative, enabling selective reactions at other functional sites in complex molecule assembly. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it ideal for multi-step syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where controlled amine reactivity is required. Also utilized in the development of agrochemicals and specialty polymers due to its reliable transformation behavior in coupling and alkylation reactions.

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Test Parameter Specification
Appearance White Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,250.00
inventory 250mg
10-20 days ฿2,600.00
inventory 1g
10-20 days ฿9,580.00
tert-Butyl (1-bromopropan-2-yl)carbamate
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It serves as a protected amine derivative, enabling selective reactions at other functional sites in complex molecule assembly. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it ideal for multi-step syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where controlled am

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It serves as a protected amine derivative, enabling selective reactions at other functional sites in complex molecule assembly. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions and can be removed under mild acidic conditions, making it ideal for multi-step syntheses. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where controlled amine reactivity is required. Also utilized in the development of agrochemicals and specialty polymers due to its reliable transformation behavior in coupling and alkylation reactions.

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