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 1346647-18-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Potassium cyclohexylmethyltrifluoroborate delivers a stable, bench-ready trifluoroborate handle for cross-coupling reactions. This reagent features a sterically protected cyclohexylmethyl moiety that enhances functional group tolerance and reduces protodeboronation. It integrates seamlessly into Suzuki-Miyaura protocols under standard conditions, enabling efficient C–C bond formation with aryl and heteroaryl halides.
Potassium cyclohexylmethyltrifluoroborate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate group offers enhanced hydrolytic stability and functional group tolerance compared to traditional boronic acids, facilitating reliable C–C bond formation under mild conditions. This reagent functions effectively in diverse coupling protocols with aryl, heteroaryl, and vinyl halides, supporting scalable synthesis of complex molecular architectures.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: