Tert-butyl 6-bromohexylcarbamate

≥95%

Reagent Code: #240213
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CAS Number 142356-33-0

science Other reagents with same CAS 142356-33-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.20 g/mol
Formula C₁₁H₂₂BrNO₂
badge Registry Numbers
MDL Number MFCD06201019
thermostat Physical Properties
Boiling Point 340.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.192 g/mL at 20 °C(lit.)
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromoalkyl chain allows for nucleophilic substitution reactions, enabling the introduction of the protected aminohexyl group into target molecules. The tert-butoxycarbonyl (Boc) protecting group ensures the amine remains inert during reactions and can be easily deprotected under mild acidic conditions when needed. Commonly employed in the synthesis of bioactive compounds, including receptor ligands and enzyme inhibitors, where a spacer arm with a terminal amine is required. Also utilized in the development of functionalized polymers and surface modifiers in material science due to its reactivity and compatibility with various coupling strategies.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,880.00
inventory 25g
10-20 days ฿12,540.00
inventory 100g
10-20 days ฿49,880.00
inventory 1g
10-20 days ฿820.00

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Tert-butyl 6-bromohexylcarbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromoalkyl chain allows for nucleophilic substitution reactions, enabling the introduction of the protected aminohexyl group into target molecules. The tert-butoxycarbonyl (Boc) protecting group ensures the amine remains inert during reactions and can be easily deprotected under mild acidic conditions when needed. Commonly employed in the synthesis of bioactive compounds, including rece

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromoalkyl chain allows for nucleophilic substitution reactions, enabling the introduction of the protected aminohexyl group into target molecules. The tert-butoxycarbonyl (Boc) protecting group ensures the amine remains inert during reactions and can be easily deprotected under mild acidic conditions when needed. Commonly employed in the synthesis of bioactive compounds, including receptor ligands and enzyme inhibitors, where a spacer arm with a terminal amine is required. Also utilized in the development of functionalized polymers and surface modifiers in material science due to its reactivity and compatibility with various coupling strategies.

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