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 1001200-60-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a 4-fluoro-3-methylphenyl group attached to a tetramethyl-substituted dioxaborolane ring, offering enhanced stability and compatibility with Suzuki-Miyaura cross-coupling reactions. The electron-deficient aryl moiety enables efficient coupling under mild conditions, while the steric protection from methyl groups minimizes protodeboronation. This bench-stable reagent streamlines access to complex biaryl architectures in synthetic and medicinal chemistry workflows.
2-(4-Fluoro-3-methylphenyl)-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 arylboronate functionality enables efficient coupling with a wide range of halides and pseudohalides under mild conditions, facilitating the construction of biaryl scaffolds common in pharmaceutical and agrochemical development. The tetramethyl-substituted dioxaborolane enhances stability and ease of purification, while the 4-fluoro-3-methylphenyl group provides a versatile handle for further functionalization.
|
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: