4-Chloro-2-(tributylstannyl)pyridine

95%

Reagent Code: #163142
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CAS Number 1204580-71-1

science Other reagents with same CAS 1204580-71-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.59 g/mol
Formula C₁₇H₃₀ClNSn
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily as an intermediate in cross-coupling reactions, especially in palladium-catalyzed reactions such as Stille coupling. It enables the formation of carbon-carbon bonds by transferring the pyridine moiety to aryl or vinyl halides, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stannyl group facilitates efficient coupling under mild conditions, offering high selectivity and yield in heterocyclic compound construction. Commonly employed in research and development for drug discovery and materials science where functionalized pyridines are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿11,030.00
1g
10-20 days ฿30,900.00
50mg
10-20 days ฿3,190.00
4-Chloro-2-(tributylstannyl)pyridine
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Used primarily as an intermediate in cross-coupling reactions, especially in palladium-catalyzed reactions such as Stille coupling. It enables the formation of carbon-carbon bonds by transferring the pyridine moiety to aryl or vinyl halides, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stannyl group facilitates efficient coupling under mild conditions, offering high selectivity and yield in heterocyclic compound construction. Commonly

Used primarily as an intermediate in cross-coupling reactions, especially in palladium-catalyzed reactions such as Stille coupling. It enables the formation of carbon-carbon bonds by transferring the pyridine moiety to aryl or vinyl halides, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stannyl group facilitates efficient coupling under mild conditions, offering high selectivity and yield in heterocyclic compound construction. Commonly employed in research and development for drug discovery and materials science where functionalized pyridines are required.

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