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 182344-14-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety features a strategically positioned fluorine atom that enhances metabolic stability and modulates electronic properties. The hydroxyl group enables efficient coupling in Suzuki-Miyaura reactions, while the overall structure offers improved solubility and bench stability under standard conditions.
(3-Fluoro-4-hydroxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. The ortho-fluoro substituent enhances metabolic stability in bioactive scaffolds, while the boronic acid and phenolic hydroxyl groups provide orthogonal reactivity for downstream functionalization. Bench-stable and readily purified by recrystallization, it facilitates robust synthesis of fluorinated arenes and heterocyclic intermediates relevant to medicinal chemistry.
|
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: