tert-Butyl(4-bromopyridin-2-yl)(cyclopropylmethyl)carbamate

98%

Reagent Code: #155539
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CAS Number 1773506-51-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.22 g/mol
Formula C₁₄H₁₉BrN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromopyridine moiety, enabling the formation of C–C and C–N bonds in drug discovery pathways. Also utilized in the preparation of protease inhibitors and receptor modulators, where the tert-butyl carbamate group acts as a protected amine, facilitating controlled deprotection during multistep syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,550.00
inventory 1g
10-20 days ฿6,890.00
inventory 100mg
10-20 days ฿1,530.00
inventory 5g
10-20 days ฿32,250.00

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tert-Butyl(4-bromopyridin-2-yl)(cyclopropylmethyl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromopyridine moiety, enabling the formation of C–C and C–N bonds in drug discovery pathways. Also utilized in the preparation of protease inhibitors and rece

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions due to the presence of the bromopyridine moiety, enabling the formation of C–C and C–N bonds in drug discovery pathways. Also utilized in the preparation of protease inhibitors and receptor modulators, where the tert-butyl carbamate group acts as a protected amine, facilitating controlled deprotection during multistep syntheses.

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