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 181585-93-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 5-nitro-1H-pyrazole-3-carboxylate features a nitro-substituted pyrazole core with a methyl ester at the 3-position, delivering a robust scaffold for heterocyclic synthesis. The electron-deficient pyrazole ring enables efficient coupling reactions, while the ester group provides a handle for further derivatization. This compound exhibits excellent stability under standard conditions and is well-suited for medicinal chemistry applications requiring precise functional group placement.
Methyl 5-nitro-1H-pyrazole-3-carboxylate serves as a versatile heterocyclic building block in medicinal chemistry and agrochemical synthesis. The nitro group at C5 enables subsequent reduction to an amino derivative, while the ester functionality supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient access to pyrazole-based scaffolds relevant to drug discovery.
|
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: