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 1373253-24-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This imidazothiadiazole carboxylic acid features a brominated heterocyclic core with enhanced reactivity at the 2-position, enabling direct coupling in C–H functionalization and cross-coupling protocols. The electron-deficient scaffold supports stable incorporation into bioactive molecules, while the carboxylic acid group facilitates conjugation or salt formation under mild conditions.
2-Bromoimidazo[2,1-b][1,3,4]thiadiazole-6-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of bioactive scaffolds. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid functionality supports derivatization via amide bond formation or esterification. Its stability under standard bench conditions and compatibility with diverse functional groups make it a practical choice for medicinal chemistry campaigns 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: