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 1334019-92-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl carbonochloridate features a boronate ester group paired with a reactive carbonate chloride handle. This combination enables efficient coupling in Suzuki-Miyaura reactions and facilitates direct installation of aryl linkages under mild conditions. The tetramethyl dioxaborolane moiety ensures stability and ease of handling, while the benzyl-carbonochloridate functionality provides rapid conjugation to nucleophiles. Ideal for modular synthesis in medicinal chemistry and materials science applications.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl carbonochloridate serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The dioxaborolane group enables efficient coupling with aryl halides under mild conditions, while the benzyl carbonochloridate moiety offers orthogonal reactivity for peptide synthesis or targeted derivatization. Bench-stable and readily handled, it facilitates rapid access to functionalized biaryl scaffolds and complex molecular architectures in medicinal chemistry and materials science workflows.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅱ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: