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 325141-71-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized nitrile integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety ensures high stability and compatibility with diverse reaction environments. The acetonitrile group provides a polar handle for downstream derivatization, enhancing utility in synthetic workflows requiring precise functional group placement.
2-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetonitrile serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The nitrile group provides orthogonal reactivity and enhanced solubility, while the tetramethyl-substituted dioxaborolane ensures excellent stability and compatibility with diverse reaction conditions. Ideal for constructing biaryl scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 3276
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H315-H319-H335
|
|
|
Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: