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 143825-84-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a phenylvinyl substituent flanked by two tetramethyl groups, enhancing stability and solubility. The dioxaborolane ring enables efficient Suzuki-Miyaura coupling under mild conditions, delivering robust cross-coupling outcomes in complex molecule synthesis.
4,4,5,5-Tetramethyl-2-(1-phenylvinyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its vinyl boronate functionality enables efficient coupling with aryl and heteroaryl halides under mild conditions, facilitating the construction of styrenyl-linked biaryls and conjugated systems. The tetramethyl-substituted dioxaborolane core enhances stability and simplifies purification, making it well-suited for iterative synthesis and late-stage functionalization in medicinal chemistry 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: