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 2454397-84-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a sterically shielded tetramethyl-1,3,2-dioxaborolane ring paired with an electron-deficient 8-chloronaphthalene moiety. It enables efficient cross-coupling under standard conditions, delivering high yields in Suzuki-Miyaura reactions. The bench-stable, moisture-tolerant structure simplifies handling and storage in synthetic workflows.
2-(8-Chloronaphthalen-1-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. The 8-chloronaphthalene moiety enables efficient C–C bond formation with diverse aryl and heteroaryl halides, facilitating the construction of biaryl scaffolds common in pharmaceutical and materials chemistry. Its tetramethyl-substituted dioxaborolane ring ensures excellent shelf stability, minimal protodeboronation, and compatibility with aqueous workups, simplifying purification and enhancing reproducibility in iterative synthesis 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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: