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 1160573-87-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Bromo-2-ethyl-4-iodobenzene features a dual halogenation pattern enabling efficient cross-coupling reactions. The bromo and iodo substituents offer orthogonal reactivity, facilitating sequential functionalization. This ortho-alkylated aryl halide exhibits enhanced solubility and stability under standard conditions, streamlining synthetic workflows in medicinal chemistry and materials science applications.
1-Bromo-2-ethyl-4-iodobenzene serves as a versatile biaryl building block in palladium-catalyzed cross-coupling reactions. The bromo and iodo substituents enable sequential functionalization, while the ethyl group provides steric and electronic modulation. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient synthesis of complex aromatic architectures relevant to pharmaceutical and materials chemistry.
|
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-P302+P352-P304+P340
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: