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 1352794-90-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized naphthalene derivative features a stable tetramethylboronate group that enables efficient Suzuki-Miyaura coupling under mild conditions. The nitrile substituent enhances electron-withdrawing character, facilitating conjugation and enabling precise functionalization in complex molecular architectures.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthonitrile serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The naphthonitrile moiety provides a rigid, electron-deficient scaffold ideal for constructing biaryl and heterocyclic frameworks. The pinacol boronate group ensures excellent stability, ease of handling, and compatibility with diverse reaction conditions, enabling efficient C–C bond formation in medicinal chemistry and materials synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: