2-Tributylstannylpyrimidine

95%

Reagent Code: #41843
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CAS Number 153435-63-3

science Other reagents with same CAS 153435-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.12 g/mol
Formula C₁₆H₃₀N₂Sn
badge Registry Numbers
MDL Number MFCD01319085
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily in organic synthesis as a reagent for cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals, enabling the introduction of pyrimidine moieties into complex molecules. Its organotin properties make it valuable in Stille reactions, facilitating the creation of biologically active compounds. Additionally, it is employed in material science for the development of organic electronic materials and ligands in catalysis.

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Test Parameter Specification
Appearance Colorless to brown liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿12,420.00
inventory 1g
10-20 days ฿3,530.00
inventory 250mg
10-20 days ฿1,400.00
inventory 25g
10-20 days ฿45,660.00

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2-Tributylstannylpyrimidine
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Used primarily in organic synthesis as a reagent for cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals, enabling the introduction of pyrimidine moieties into complex molecules. Its organotin properties make it valuable in Stille reactions, facilitating the creation of biologically active compounds. Additionally, it is employed in material science for the development of organic electronic m

Used primarily in organic synthesis as a reagent for cross-coupling reactions, particularly in the formation of carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals, enabling the introduction of pyrimidine moieties into complex molecules. Its organotin properties make it valuable in Stille reactions, facilitating the creation of biologically active compounds. Additionally, it is employed in material science for the development of organic electronic materials and ligands in catalysis.

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