4-(Tributylstannyl)pyrimidine

95%

Reagent Code: #240875
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CAS Number 332133-92-3

science Other reagents with same CAS 332133-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.13 g/mol
Formula C₁₆H₃₀N₂Sn
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in palladium-catalyzed cross-coupling reactions, such as the Stille reaction, to introduce pyrimidine rings into complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials where pyrimidine-based structures are needed. Its organotin group facilitates efficient carbon-carbon bond formation under mild conditions, offering good selectivity and compatibility with various functional groups. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocyclic systems found in bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿16,000.00
inventory 5g
10-20 days ฿69,280.00
inventory 10g
10-20 days ฿124,800.00
4-(Tributylstannyl)pyrimidine
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Used primarily as an intermediate in palladium-catalyzed cross-coupling reactions, such as the Stille reaction, to introduce pyrimidine rings into complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials where pyrimidine-based structures are needed. Its organotin group facilitates efficient carbon-carbon bond formation under mild conditions, offering good selectivity and compatibility with various functional groups. Commonly applied in

Used primarily as an intermediate in palladium-catalyzed cross-coupling reactions, such as the Stille reaction, to introduce pyrimidine rings into complex organic molecules. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials where pyrimidine-based structures are needed. Its organotin group facilitates efficient carbon-carbon bond formation under mild conditions, offering good selectivity and compatibility with various functional groups. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocyclic systems found in bioactive compounds.

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