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 15366-65-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Iodonicotinic acid delivers a versatile iodinated pyridine scaffold for cross-coupling and bioconjugation applications. The carboxylic acid functionality enables direct derivatization, while the para-iodo group facilitates palladium-catalyzed transformations. This bench-stable, moisture-tolerant reagent integrates seamlessly into synthetic workflows requiring orthogonal functional handles.
5-Iodonicotinic acid serves as a versatile building block for the synthesis of iodinated heterocycles and bioactive molecules. Its iodine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates direct derivatization or conjugation. The compound exhibits good bench stability and compatibility with standard synthetic protocols, enabling efficient access to functionalized nicotinate scaffolds in medicinal chemistry and materials science applications.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: