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 850568-48-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronic acid features a hydroxypropyl chain appended to the phenyl ring, enhancing solubility and enabling precise functionalization in Suzuki-Miyaura coupling reactions. The pendant hydroxyl group supports hydrogen bonding and facilitates derivatization under mild conditions.
(4-(3-Hydroxypropyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The pendant hydroxyl group provides orthogonal functionality for further derivatization, while the boronic acid moiety exhibits excellent bench stability and compatibility with diverse functional groups. Its well-defined reactivity profile makes it particularly valuable for constructing biaryl architectures in medicinal chemistry and materials science applications.
|
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: