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 41806-40-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Methyl-1H-imidazole-5-carboxylic acid features a polar, electron-deficient imidazole core paired with a carboxylic acid group, enabling direct conjugation in peptide and heterocyclic synthesis. This bench-stable derivative integrates readily into bioactive scaffolds requiring nitrogen-rich, hydrogen-bond-capable motifs under standard conditions.
1-Methyl-1H-imidazole-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of imidazole-based scaffolds prevalent in bioactive molecules. Its carboxylic acid functionality facilitates direct amidation, esterification, and coupling reactions under standard conditions. The methylated imidazole ring enhances metabolic stability and modulates electronic properties, while maintaining excellent bench stability and ease of purification—key advantages for high-throughput screening and process-scale applications.
|
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: