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 16188-57-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Iodo-4-methylphenol serves as a valuable aryl iodide building block for cross-coupling reactions, featuring a sterically accessible iodine atom paired with an electron-rich methyl-substituted phenolic ring. This combination enables efficient palladium-catalyzed transformations under standard conditions, delivering functionalized arenes with high regioselectivity and minimal side-product formation.
2-Iodo-4-methylphenol serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable aryl iodide functionality. The ortho-iodo and para-methyl substituents provide favorable electronic and steric profiles for C–C bond formation. Its bench-stable nature and compatibility with standard coupling protocols make it a practical choice for constructing biaryl scaffolds 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-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: