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 1071924-13-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester features a sterically shielded aryl group that enhances stability and minimizes protodeboronation. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and compatibility with diverse coupling conditions. Ideal for Suzuki-Miyaura cross-couplings requiring robust, moisture-tolerant reagents.
2-(3,5-Di-tert-butylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a sterically protected boronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-di-tert-butyl substitution enhances stability and minimizes protodeboronation, enabling reliable coupling under mild conditions. The tetramethyl-substituted dioxaborolane ring offers excellent bench stability and ease of purification, facilitating its use in complex molecule assembly and API intermediate synthesis.
|
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: