tert-Butyl N-(6-fluoropyridin-2-yl)carbamate

≥95%

Reagent Code: #82908
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CAS Number 891856-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.22 g/mol
Formula C₁₀H₁₃FN₂O₂
badge Registry Numbers
MDL Number MFCD11976435
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring a fluoropyridine moiety and a tert-butyl carbamate group, makes it valuable in pharmaceutical research, particularly in the design of drug candidates. The fluorine atom enhances the molecule's reactivity and binding affinity, which is useful in creating biologically active molecules. It is often employed in the synthesis of agrochemicals and active pharmaceutical ingredients (APIs), where the fluoropyridine ring plays a critical role in improving the efficacy and stability of the final product. Additionally, its tert-butyl carbamate group serves as a protective group in peptide synthesis, ensuring selective reactions during complex molecular constructions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $304.53
tert-Butyl N-(6-fluoropyridin-2-yl)carbamate
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex compounds. Its structure, featuring a fluoropyridine moiety and a tert-butyl carbamate group, makes it valuable in pharmaceutical research, particularly in the design of drug candidates. The fluorine atom enhances the molecule's reactivity and binding affinity, which is useful in creating biologically active molecules. It is often employed in the synthesis of agrochemicals and active pharmaceutical ingredients (APIs), where the fluoropyridine ring plays a critical role in improving the efficacy and stability of the final product. Additionally, its tert-butyl carbamate group serves as a protective group in peptide synthesis, ensuring selective reactions during complex molecular constructions.
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