tert-Butyl (3-(bromomethyl)phenyl)carbamate

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Reagent Code: #145332
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CAS Number 118684-32-5

science Other reagents with same CAS 118684-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.17 g/mol
Formula C₁₂H₁₆BrNO₂
thermostat Physical Properties
Melting Point 122°C
Boiling Point 309.0±25.0°C
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. The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, enabling the introduction of various side chains. The tert-butyl carbamate moiety serves as a protected amine, which can be deprotected under mild conditions to release the corresponding amine for use in subsequent reactions. Commonly employed in the synthesis of bioactive molecules, including kinase inhibitors and other therapeutic agents. Its structure facilitates the construction of complex aromatic amines found in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿930.00
inventory 5g
10-20 days ฿4,610.00
inventory 10g
10-20 days ฿9,200.00
inventory 25g
10-20 days ฿23,000.00

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tert-Butyl (3-(bromomethyl)phenyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, enabling the introduction of various side chains. The tert-butyl carbamate moiety serves as a protected amine, which can be deprotected under mild conditions to release the corresponding amine for use in subsequent reactions. Commonly employed in the synthesis of bioactive molecules, incl

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, enabling the introduction of various side chains. The tert-butyl carbamate moiety serves as a protected amine, which can be deprotected under mild conditions to release the corresponding amine for use in subsequent reactions. Commonly employed in the synthesis of bioactive molecules, including kinase inhibitors and other therapeutic agents. Its structure facilitates the construction of complex aromatic amines found in drug candidates.

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