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 493035-82-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Hydroxy-2-methylbenzeneboronic acid features a boronic acid group ortho to a phenolic hydroxyl, enabling efficient Suzuki-Miyaura coupling under mild conditions. The methyl substituent enhances stability and modulates electronic properties, while the hydroxyl group facilitates solubility and directional coordination in complex synthesis. This compound serves as a key building block for bioactive heterocycles and functionalized arenes in medicinal chemistry and materials science.
4-Hydroxy-2-methylbenzeneboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its ortho-hydroxyl group enhances solubility and facilitates directed functionalization, while the boronic acid moiety offers reliable reactivity under mild conditions. The methyl group provides steric control and metabolic stability, making this compound valuable for medicinal chemistry and materials synthesis.
|
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: