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 37566-40-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Chloro-1,3,4-thiadiazol-2-amine features a chlorinated thiadiazole core with a primary amine group, delivering enhanced reactivity for heterocyclic functionalization. This bench-stable scaffold integrates readily into bioactive molecule design, particularly in agrochemical and pharmaceutical applications, where its electron-deficient ring system supports targeted interactions.
5-Chloro-1,3,4-thiadiazol-2-amine serves as a versatile heterocyclic building block in medicinal chemistry and materials science. Its chloro substituent enables electrophilic functionalization, while the thiadiazole core offers robust stability and favorable electronic properties. The amine group facilitates coupling reactions, including amidation and alkylation, supporting diverse derivatization strategies. This compound demonstrates excellent bench stability and compatibility with standard purification methods, making it a reliable reagent for constructing bioactive scaffolds and functionalized polymers.
|
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: