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 626-41-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3,5-Dibromophenol features two bromine atoms at the 3 and 5 positions of the phenolic ring, creating a highly electron-deficient aromatic system. This configuration enhances its utility in palladium-catalyzed cross-coupling reactions, where the bromo groups serve as effective coupling handles. The compound exhibits excellent stability under standard bench conditions and integrates readily into complex molecular architectures.
3,5-Dibromophenol serves as a valuable building block in medicinal chemistry and materials science, enabling direct functionalization at the ortho positions relative to the phenolic hydroxyl. Its bromine substituents facilitate palladium-catalyzed cross-coupling reactions, including Suzuki and Stille couplings, with high regioselectivity. The compound exhibits excellent bench stability and ease of purification, making it well-suited for multi-step synthesis workflows requiring reliable reactivity and functional group compatibility.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: