tert-Butyl (5-bromo-2-chloropyridin-4-yl)carbamate

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Reagent Code: #130604
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CAS Number 1820683-84-8

science Other reagents with same CAS 1820683-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.57 g/mol
Formula C₁₀H₁₂BrClN₂O₂
badge Registry Numbers
MDL Number MFCD26936360
thermostat Physical Properties
Boiling Point 310.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.539±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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 molecules for drug discovery. Commonly employed in cross-coupling reactions due to the presence of halogen atoms, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides. The tert-butyl carbamate group acts as a protecting group for amines, facilitating controlled reactivity during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,660.00
inventory 250mg
10-20 days ฿11,310.00

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tert-Butyl (5-bromo-2-chloropyridin-4-yl)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 molecules for drug discovery. Commonly employed in cross-coupling reactions due to the presence of halogen atoms, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides

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 molecules for drug discovery. Commonly employed in cross-coupling reactions due to the presence of halogen atoms, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides. The tert-butyl carbamate group acts as a protecting group for amines, facilitating controlled reactivity during multi-step syntheses.

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