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 106120-04-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromobenzene-1,3-diol features a bromine substituent at the para position relative to one hydroxyl group, creating a distinct electronic profile that enhances reactivity in cross-coupling and functionalization reactions. The two adjacent hydroxyl groups enable strong hydrogen bonding and solubility in polar solvents, facilitating use in synthetic transformations under standard conditions. This compound serves as a valuable intermediate for pharmaceutical and agrochemical synthesis.
5-Bromobenzene-1,3-diol serves as a versatile building block for the synthesis of functionalized aromatic scaffolds. Its ortho-dihydroxy arrangement enables efficient metal-catalyzed cross-coupling reactions, while the bromine substituent provides a reliable handle for further derivatization via palladium-mediated transformations. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for applications in 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: