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 376584-76-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester integrates a benzo[b]thiophene moiety with a stable, bench-ready dioxaborolane core. It enables efficient Suzuki-Miyaura coupling under standard conditions, delivering fused heterocyclic architectures with high functional group tolerance and minimal byproduct formation.
2-(Benzo[b]thiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its benzo[b]thiophene moiety enables efficient construction of biaryl scaffolds prevalent in pharmaceutical and agrochemical research. The tetramethyl-substituted dioxaborolane enhances shelf stability and minimizes protodeboronation, while facilitating straightforward purification and compatibility with diverse 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-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: