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 867333-43-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a cyano group ortho to the boronate, enhancing electrophilicity and enabling efficient cross-coupling. The methyl substituent provides steric control and improves solubility in organic media. Bench-stable under standard conditions, it integrates readily into Suzuki-Miyaura reactions for aryl-aryl bond formation.
(5-Cyano-2-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds with high functional group tolerance. The nitrile and methyl groups provide orthogonal reactivity for downstream derivatization, while the boronic acid moiety offers excellent bench stability and ease of purification. This compound facilitates access to substituted heterocycles and complex architectures relevant to medicinal chemistry and materials science.
|
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: