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 1951466-68-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Chloro-2-methyl-2H-pyrazolo[3,4-c]pyridine features a fused bicyclic core with a chlorine substituent at the 5-position and a methyl group at the 2-position, conferring enhanced electron-withdrawing character and improved metabolic stability. This scaffold serves as a critical building block in medicinal chemistry for targeted kinase inhibition and CNS-active compound development, offering high reactivity in cross-coupling transformations under mild conditions.
5-Chloro-2-methyl-2H-pyrazolo[3,4-c]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its electron-deficient pyrazolopyridine core enables efficient coupling reactions via the chloro substituent, while the methyl group provides steric and electronic modulation. The scaffold exhibits bench stability and compatibility with Pd-catalyzed cross-coupling, Suzuki-Miyaura, and Buchwald-Hartwig transformations, facilitating rapid diversification in drug discovery campaigns.
|
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: