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 1427460-96-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 7-bromo-1H-indazole-5-carboxylate features a brominated indazole core with a methyl ester at the 5-position, enabling direct functionalization in cross-coupling and derivatization workflows. The electron-deficient heterocycle pairs effectively with palladium catalysts, while the ester group offers synthetic handle versatility under standard conditions.
Methyl 7-bromo-1H-indazole-5-carboxylate serves as a versatile building block for the synthesis of indazole-based pharmaceutical intermediates. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports selective transformations including hydrolysis and reduction. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthetic sequences in medicinal chemistry and API development.
|
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: