tert-butyl ((1-(4-(tert-butyl)phenyl)cyclobutyl)methyl)carbamate

90%

Reagent Code: #241953

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.47 g/mol
Formula C₂₀H₃₁NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protected amine building block for the development of complex molecules, including drug candidates targeting central nervous system disorders and inflammatory diseases. The tert-butyl carbamate (Boc) group provides stability during synthesis and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its sterically hindered structure also helps control regioselectivity in coupling reactions, making it valuable in the preparation of highly substituted cyclobutane derivatives with potential biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,400.00
inventory 250mg
10-20 days ฿5,760.00

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tert-butyl ((1-(4-(tert-butyl)phenyl)cyclobutyl)methyl)carbamate
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protected amine building block for the development of complex molecules, including drug candidates targeting central nervous system disorders and inflammatory diseases. The tert-butyl carbamate (Boc) group provides stability during synthesis and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its sterically hindered struct

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It serves as a protected amine building block for the development of complex molecules, including drug candidates targeting central nervous system disorders and inflammatory diseases. The tert-butyl carbamate (Boc) group provides stability during synthesis and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its sterically hindered structure also helps control regioselectivity in coupling reactions, making it valuable in the preparation of highly substituted cyclobutane derivatives with potential biological activity.

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