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 1105039-93-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This pyrazole derivative features a methoxybenzyl group that enhances solubility and stability in organic media. The carboxylic acid moiety enables direct conjugation or derivatization in synthetic routes. Designed for use in medicinal chemistry, it integrates readily into bioactive scaffolds requiring polar, electron-rich functionalities.
1-(4-Methoxybenzyl)-1H-pyrazole-4-carboxylic acid serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient functionalization at the pyrazole core. The carboxylic acid group facilitates direct coupling reactions, while the 4-methoxybenzyl moiety provides bench stability and orthogonal protection potential. This compound exhibits excellent functional group tolerance and is compatible with standard amide bond formation, Suzuki coupling, and reductive deprotection protocols, making it ideal for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active scaffolds.
|
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: