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 20776-55-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-amino-3-iodobenzoic acid features a strategically positioned iodine atom adjacent to a carboxylic acid group, enabling direct functionalization in cross-coupling reactions. The electron-rich amino substituent enhances reactivity in palladium-catalyzed transformations. This bench-stable derivative serves as a key building block for bioactive heterocycles and pharmaceutical intermediates.
2-Amino-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-iodo group facilitates reliable coupling under standard conditions, while the amino and carboxylic acid functionalities offer complementary handles for further derivatization. Bench-stable and readily purified, it functions effectively in medicinal chemistry and process 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-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: