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 1186403-17-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(3-Bromo-5-chlorophenyl)boronic acid features a dual halogenated aryl scaffold enabling efficient cross-coupling in Suzuki-Miyaura reactions. The boronic acid moiety integrates readily into complex molecular architectures, while the bromo and chloro substituents offer orthogonal reactivity for sequential functionalization. This compound exhibits bench-stable handling and compatibility with diverse reaction conditions.
(3-Bromo-5-chlorophenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. Its compatibility with both bromo and chloro leaving groups allows for sequential functionalization or selective coupling in complex molecule synthesis. The boronic acid moiety offers excellent bench stability, ease of purification, and tolerance to a range of functional groups, 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: