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 64837-49-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate features a chlorinated thiadiazole core that imparts enhanced electrophilicity and stability under standard conditions. This bench-stable reagent integrates readily into heterocyclic synthesis, serving as a key scaffold for medicinal chemistry applications.
Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to functionalized thiadiazole scaffolds. Its chloro substituent facilitates nucleophilic substitution reactions, while the ester group supports further transformations such as hydrolysis or coupling. The molecule exhibits good bench stability and is compatible with standard reaction conditions, making it valuable for medicinal chemistry and materials science 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: