Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 458532-86-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine delivers a boronate handle at the pyridine 4-position, enabling palladium-catalyzed cross-coupling under standard conditions. The fluorine substituent enhances electronic modulation and metabolic stability. This bench-stable reagent integrates efficiently into complex molecular architectures with minimal side reactivity.
2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate ester building block for palladium-catalyzed cross-coupling reactions. Its fluoropyridine core enables selective functionalization in medicinal chemistry and materials science. The tetramethyl-substituted dioxaborolane moiety ensures excellent bench stability, mild reaction conditions, and high tolerance to diverse functional groups, facilitating efficient synthesis of biaryl scaffolds and complex heterocycles.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H319
|
|
|
Precautionary Statements : P264-P270-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: