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 403-18-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Fluoro-3-iodobenzoic acid features a strategically positioned iodine atom enabling efficient cross-coupling reactions, while the fluorine substituent enhances electronic modulation and metabolic stability. This ortho-halogenated scaffold delivers high reactivity in palladium-catalyzed transformations under standard conditions, making it ideal for constructing complex aromatic architectures in medicinal chemistry and materials science applications.
4-Fluoro-3-iodobenzoic acid serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The ortho-fluoro and iodo substituents provide complementary reactivity for sequential functionalization, while the carboxylic acid group allows for direct derivatization or salt formation. Bench-stable and compatible with standard synthetic workflows, it facilitates rapid access to complex aromatic systems in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301
|
|
|
Precautionary Statements : P264-P270-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: