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 20942-70-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-(tert-Butyl)-2-iodophenol features a sterically hindered tert-butyl group flanking a reactive iodophenol motif, enabling selective cross-coupling under mild conditions. This bench-stable derivative delivers high functional group tolerance and efficient integration into complex molecular architectures via palladium-catalyzed transformations.
5-(tert-Butyl)-2-iodophenol serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki and Stille reactions due to its stable aryl iodide functionality. The electron-donating tert-butyl group enhances solubility and reduces oxidative degradation, while the phenolic hydroxyl facilitates orthogonal derivatization. This compound exhibits excellent bench stability and is compatible with standard purification protocols, making it ideal for constructing complex heterocyclic scaffolds and functionalized arenes in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: