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 891270-35-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates a pyrazole-phenyl scaffold, delivering enhanced stability and solubility in polar solvents. The electron-deficient aryl ring enables efficient Suzuki-Miyaura coupling under mild conditions, facilitating rapid assembly of biaryl architectures in medicinal chemistry and materials synthesis.
(4-(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 under mild conditions. Its stability in air and moisture facilitates handling and purification, while the pyrazole moiety provides enhanced solubility and metabolic stability. The boronic acid functional group exhibits broad compatibility with diverse coupling partners, making it a reliable reagent for synthesizing functionalized arylated heterocycles used in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H315-H318-H335
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: