4-(Trimethylsilyl)pyridin-3-yl trifluoromethanesulfonate

97%

Reagent Code: #242371
fingerprint
CAS Number 1211583-40-2

science Other reagents with same CAS 1211583-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.34 g/mol
Formula C₉H₁₂F₃NO₃SSi
badge Registry Numbers
MDL Number MFCD18257070
inventory_2 Storage & Handling
Density 1.259 at 25 °C
Storage 2-8°C, sealed, dry, inflatable

description Product Description

Used as a key intermediate in cross-coupling reactions, particularly in palladium-catalyzed transformations such as Suzuki-Miyaura and Stille couplings. Its triflate group acts as an excellent leaving group, enabling efficient formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The trimethylsilyl group can be selectively removed or further functionalized, adding versatility in multi-step synthetic routes. Commonly employed in the preparation of pyridine-based compounds where controlled substitution is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,090.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(Trimethylsilyl)pyridin-3-yl trifluoromethanesulfonate
No image available

Used as a key intermediate in cross-coupling reactions, particularly in palladium-catalyzed transformations such as Suzuki-Miyaura and Stille couplings. Its triflate group acts as an excellent leaving group, enabling efficient formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The trimethylsilyl group can be selectively removed or further functionalized, adding versatility in multi-step synthetic routes. Commonly employed in the pr

Used as a key intermediate in cross-coupling reactions, particularly in palladium-catalyzed transformations such as Suzuki-Miyaura and Stille couplings. Its triflate group acts as an excellent leaving group, enabling efficient formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The trimethylsilyl group can be selectively removed or further functionalized, adding versatility in multi-step synthetic routes. Commonly employed in the preparation of pyridine-based compounds where controlled substitution is required.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...