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 40253-47-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 5-methyl-1H-1,2,4-triazole-3-carboxylate features a bench-stable triazole core with a methyl substituent at the C5 position and an ethyl ester group at C3. This combination imparts enhanced solubility in organic solvents and facilitates direct incorporation into heterocyclic scaffolds. The electron-deficient triazole ring enables efficient coupling reactions, making it a valuable building block for medicinal chemistry and materials synthesis.
Ethyl 5-methyl-1H-1,2,4-triazole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to triazolyl scaffolds prevalent in medicinal chemistry. The ethyl ester group facilitates nucleophilic acyl substitution and subsequent derivatization, while the 5-methyl substituent enhances metabolic stability. Its bench-stable nature and compatibility with standard coupling conditions make it suitable for iterative synthetic strategies and API intermediate 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: