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 850623-36-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Potassium (4-cyanophenyl)trifluoroborate delivers a stable, bench-tolerant boronate moiety paired with a para-cyano group, enabling direct Suzuki-Miyaura coupling without preactivation. This reagent integrates seamlessly into synthetic workflows requiring electron-deficient aryl transfer, offering high functional group tolerance and reliable yields under standard conditions.
Potassium (4-cyanophenyl)trifluoroborate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. Its cyano group enhances electrophilic reactivity and enables downstream transformations such as amidation or hydrolysis. The trifluoroborate moiety offers excellent functional group tolerance and compatibility with diverse reaction conditions, facilitating efficient construction of biaryl scaffolds in medicinal chemistry and materials science applications.
|
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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: