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 1030625-44-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4,7-Diiodobenzo[d][1,3]dioxole serves as a high-performance coupling partner in palladium-catalyzed cross-coupling reactions. The dual iodide substituents enable efficient functionalization at both positions, while the rigid, electron-rich dioxole core enhances stability and reactivity under standard conditions. This compound integrates seamlessly into complex molecular architectures requiring precise spatial control and enhanced electronic tuning.
4,7-Diiodobenzo[d][1,3]dioxole serves as a versatile diarylated building block in palladium-catalyzed cross-coupling reactions. Its rigid, electron-rich heteroaromatic core exhibits excellent stability under standard reaction conditions and enables efficient C–C bond formation with boronic acids, stannanes, and other coupling partners. The iodine substituents provide high reactivity in Suzuki, Stille, and Negishi couplings, facilitating rapid access to complex biaryl architectures. Ideal for medicinal chemistry and materials synthesis, it offers predictable regioselectivity and clean purification profiles.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: