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 129295-32-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Chloro-1H-indazole-3-carboxylic acid is a bench-stable heterocyclic scaffold featuring a chlorine substituent at the 7-position and a carboxylic acid group at the 3-position. This combination imparts enhanced electron-withdrawing character and improved solubility in polar solvents, enabling direct incorporation into bioactive molecule synthesis.
7-Chloro-1H-indazole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into bioactive heterocycles via standard coupling reactions. Its carboxylic acid functionality facilitates amide and ester formation under mild conditions, while the chlorinated indazole core provides enhanced metabolic stability and π-stacking potential. Bench-stable and readily purified by recrystallization, it functions reliably in peptide-like conjugations and scaffold diversification for drug discovery 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: