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 904310-72-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester-functionalized benzoic acid integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering high efficiency under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety ensures excellent stability and moisture tolerance, while the para-chloro substituent enables selective functionalization. This bench-stable reagent streamlines access to complex aryl architectures in synthetic and medicinal chemistry workflows.
3-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid serves as a versatile Suzuki-Miyaura coupling partner, enabling efficient C–C bond formation under mild conditions. The boronic ester group exhibits excellent stability, facilitates straightforward purification, and tolerates a range of functional groups. This compound functions as a key building block for the synthesis of biaryl scaffolds 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: