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 1072946-39-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2,6-Dichlorobenzyl)boronic acid features a sterically protected boronic acid moiety attached to a dichlorinated benzyl scaffold, enabling reliable coupling in Suzuki-Miyaura reactions. The electron-withdrawing chlorine substituents enhance reactivity while maintaining bench-stable handling under standard conditions. This compound integrates seamlessly into complex molecular architectures requiring orthogonal functionalization.
(2,6-Dichlorobenzyl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-dichloro substitution enhances electrophilic reactivity in downstream functionalization while maintaining compatibility with diverse reaction conditions. The boronic acid functionality enables efficient coupling with aryl and vinyl halides, facilitating rapid access to substituted biaryl architectures common in pharmaceutical and agrochemical scaffolds.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: