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 2096996-99-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,3-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group conjugated to a fluorinated pyridine core, enabling efficient Suzuki-Miyaura coupling under standard conditions. The electron-deficient heterocycle enhances reactivity, while the tetramethyl-substituted dioxaborolane imparts stability and solubility in organic media.
2,3-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The difluoropyridine core enables selective functionalization and enhances metabolic stability in medicinal chemistry applications. The pinacol boronate ester group offers excellent bench stability, facile handling, and compatibility with a broad range of coupling partners under standard reaction conditions.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: