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 74128-84-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-1-iodo-3-methoxybenzene features a strategically positioned methoxy group that enhances solubility and directs electrophilic substitution. The orthogonal halogenation pattern enables sequential cross-coupling reactions, while the bench-stable aryl iodide serves as a reliable coupling partner in palladium-catalyzed transformations.
2-Bromo-1-iodo-3-methoxybenzene serves as a versatile dihalogenated aromatic building block for palladium-catalyzed cross-coupling reactions. The ortho-bromine and meta-iodine substituents enable sequential functionalization with high chemoselectivity, while the methoxy group provides moderate electron donation and enhances solubility. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for the construction of complex substituted arenes in medicinal chemistry and materials synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H332-H335
|
|
|
Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: