tert-Butyl (5-bromopyridin-2-yl)(methyl)carbamate

95%

Reagent Code: #146079
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CAS Number 227939-01-7

science Other reagents with same CAS 227939-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.15 g/mol
Formula C₁₁H₁₅BrN₂O₂
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 bioactive molecules. 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 bromine moiety, enabling the formation of C–C and C–N bonds. Also utilized in agrochemical research for designing novel active ingredients. The tert-butyl carbamate group acts as a protecting group for amines, facilitating controlled reactivity during multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿360.00
250mg
10-20 days ฿800.00
1g
10-20 days ฿3,110.00
tert-Butyl (5-bromopyridin-2-yl)(methyl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. 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 bromine moiety, enabling the formation of C–C and C–N bonds. Also utilized in agrochemical research for designing novel active ingredients. The tert-butyl carbamate gro

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. 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 bromine moiety, enabling the formation of C–C and C–N bonds. Also utilized in agrochemical research for designing novel active ingredients. The tert-butyl carbamate group acts as a protecting group for amines, facilitating controlled reactivity during multi-step syntheses.

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