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 1378876-49-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Amino-4-bromothiophene-2-carboxamide features a brominated thiophene core with strategically positioned amino and carboxamide groups, enabling direct integration into heterocyclic scaffolds. This bench-stable compound serves as a key intermediate for synthesizing bioactive molecules in medicinal chemistry and materials science applications.
3-Amino-4-bromothiophene-2-carboxamide serves as a versatile building block in medicinal chemistry, enabling efficient access to functionalized thiophene scaffolds. The amino and carboxamide groups provide orthogonal handles for coupling reactions, while the bromine facilitates palladium-catalyzed cross-couplings. Its bench-stable nature and compatibility with standard purification methods make it ideal for multi-step synthesis of heterocyclic compounds and API intermediates.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: