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 476620-22-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a pyrazole-phenyl scaffold enabling efficient cross-coupling in Suzuki-Miyaura reactions. The ortho-substituted arylboron moiety enhances reactivity and stability under standard conditions, while the nitrogen-rich heterocycle improves solubility and functional group tolerance.
(3-(1H-Pyrazol-1-yl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds with retained heterocyclic functionality. The pyrazole moiety enhances solubility and provides a handle for further derivatization, while the boronic acid group exhibits good bench stability and compatibility with diverse reaction conditions. This compound facilitates the synthesis of complex heteroaromatic systems relevant to medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3259
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H318
|
|
|
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: