(R)-tert-Butyl 3-((6-bromopyridin-2-yl)oxy)pyrrolidine-1-carboxylate

95%

Reagent Code: #228624
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CAS Number 1261234-93-8

science Other reagents with same CAS 1261234-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.22 g/mol
Formula C₁₄H₁₉BrN₂O₃
badge Registry Numbers
MDL Number MFCD18380348
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral pyrrolidine structure with a bromopyridine moiety enables selective reactions in drug discovery, making it valuable for constructing complex molecules with high stereochemical purity. Commonly employed in cross-coupling reactions due to the bromine substituent, allowing for carbon–carbon bond formation in advanced intermediates. Also utilized in research settings to develop potential treatments for inflammatory diseases and cancer.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,560.00

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(R)-tert-Butyl 3-((6-bromopyridin-2-yl)oxy)pyrrolidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral pyrrolidine structure with a bromopyridine moiety enables selective reactions in drug discovery, making it valuable for constructing complex molecules with high stereochemical purity. Commonly employed in cross-coupling reactions due to the bromine substituent, allowing for carbon–carbon bond formation in advanced intermediates. Als

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral pyrrolidine structure with a bromopyridine moiety enables selective reactions in drug discovery, making it valuable for constructing complex molecules with high stereochemical purity. Commonly employed in cross-coupling reactions due to the bromine substituent, allowing for carbon–carbon bond formation in advanced intermediates. Also utilized in research settings to develop potential treatments for inflammatory diseases and cancer.

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