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 51158-94-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Lutidine tetrafluoroborate delivers a sterically shielded, electron-rich nitrogen center ideal for directing regioselective functionalization in catalytic processes. This bench-stable salt features enhanced solubility in polar aprotic solvents and maintains reactivity under standard conditions, enabling precise control in synthetic transformations.
2,6-Lutidine tetrafluoroborate serves as a robust, bench-stable nitrogen source in transition metal-catalyzed cross-coupling reactions. Its sterically hindered tertiary amine functionality enhances selectivity in palladium-catalyzed transformations while minimizing unwanted coordination. The tetrafluoroborate counterion facilitates solubility and stability, enabling efficient coupling with aryl halides and triflates under mild conditions. This reagent functions effectively in the synthesis of complex heterocyclic scaffolds and pharmaceutical intermediates, offering predictable reactivity and straightforward purification.
|
GHS Pictogram :
|
GHS No : GHS07,GHS05
|
|
Signal Word : Danger
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P310-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: