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 221681-75-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Chloro-1H-indazol-5-amine is a bench-stable heterocyclic amine featuring a chlorine substituent at the 6-position and a primary amine at the 5-position. This electron-deficient scaffold integrates readily into pharmaceutical intermediates, enabling efficient coupling reactions in medicinal chemistry. The para-chloro functionality enhances reactivity in cross-coupling processes, while the indazolyl core provides structural rigidity for targeted bioactive molecule design.
6-Chloro-1H-indazol-5-amine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient construction of indazole-based scaffolds. Its chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the primary amine allows for direct derivatization via acylation, alkylation, or Ullmann-type coupling. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for high-throughput screening and API development 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: