tert-Butyl (5-bromopentyl)carbamate

95%

Reagent Code: #148339
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CAS Number 83948-54-3

science Other reagents with same CAS 83948-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.18 g/mol
Formula C₁₀H₂₀BrNO₂
badge Registry Numbers
MDL Number MFCD03425513
thermostat Physical Properties
Boiling Point 324.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.214g/cm3
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions or nucleophilic substitutions, enabling the introduction of nitrogen-containing groups via the protected amine. Commonly employed in the construction of complex molecules where a protected aminoalkyl chain is required. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it valuable in multi-step synthesis. Also utilized in the development of ligands, functionalized polymers, and bioactive compound derivatives.

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Test Parameter Specification
Appearance White to Yellow Solid or Colorless to Yellow Liquid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿214.50
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿2,660.00
inventory 5g
10-20 days ฿7,810.00

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tert-Butyl (5-bromopentyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions or nucleophilic substitutions, enabling the introduction of nitrogen-containing groups via the protected amine. Commonly employed in the construction of complex molecules where a protected aminoalkyl chain is required. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild ac

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions or nucleophilic substitutions, enabling the introduction of nitrogen-containing groups via the protected amine. Commonly employed in the construction of complex molecules where a protected aminoalkyl chain is required. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it valuable in multi-step synthesis. Also utilized in the development of ligands, functionalized polymers, and bioactive compound derivatives.

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