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 408492-27-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized pyridine integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The 2,6-dichloro substitution pattern enables selective functionalization, while the tetramethyl-1,3,2-dioxaborolane moiety provides enhanced stability and reactivity.
2,6-Dichloro-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 pyridine core provides orthogonal reactivity, while the 2,6-dichloro substitution pattern enables sequential functionalization. The pinacol boronate ester offers excellent bench stability, minimal hydrolysis, and compatibility with diverse reaction conditions, facilitating efficient construction of biaryl and heteroaryl scaffolds in medicinal chemistry and materials science workflows.
|
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: