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 1309981-13-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The methyl-substituted pyrazine ring enhances electron deficiency and improves stability under standard conditions.
(6-Methylpyrazin-2-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its pyrazine core provides enhanced stability and solubility compared to related heterocycles, while the boronic acid functionality offers reliable reactivity in Suzuki–Miyaura coupling protocols. The methyl group at the 6-position imparts favorable electronic tuning and steric profile, facilitating selective transformations in complex molecule synthesis. Ideal for medicinal chemistry and materials science applications requiring robust heteroaromatic scaffolds.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: