tert-Butyl 4-(bromomethyl)benzylcarbamate

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Reagent Code: #146195
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CAS Number 187283-17-6

science Other reagents with same CAS 187283-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.19 g/mol
Formula C₁₃H₁₈BrNO₂
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 bioactive molecules. The compound’s bromomethyl group allows for nucleophilic substitution reactions, enabling the introduction of various functional groups. It is commonly employed in the construction of peptidomimetics and targeted protein degraders, such as PROTACs, due to the presence of a handle for linker attachment. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity. Its stability under a range of conditions and clean deprotection profile make it valuable in medicinal chemistry workflows.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿900.00
inventory 1g
10-20 days ฿1,560.00
inventory 5g
10-20 days ฿6,530.00
inventory 10g
10-20 days ฿13,010.00
inventory 25g
10-20 days ฿28,260.00

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tert-Butyl 4-(bromomethyl)benzylcarbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. The compound’s bromomethyl group allows for nucleophilic substitution reactions, enabling the introduction of various functional groups. It is commonly employed in the construction of peptidomimetics and targeted protein degraders, such as PROTACs, due to the presence of a handle for linker attachment. The tert-butyl carbamate (Boc) group provides amine protection during multi-step synth
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. The compound’s bromomethyl group allows for nucleophilic substitution reactions, enabling the introduction of various functional groups. It is commonly employed in the construction of peptidomimetics and targeted protein degraders, such as PROTACs, due to the presence of a handle for linker attachment. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity. Its stability under a range of conditions and clean deprotection profile make it valuable in medicinal chemistry workflows.
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