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 24287-95-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromothiophene-3-carboxylic acid features a brominated thiophene core paired with a carboxylic acid functional group, enabling direct incorporation into cross-coupling reactions and heterocyclic synthesis. This bench-stable reagent integrates readily into pharmaceutical and agrochemical scaffolds, offering high reactivity under standard conditions.
2-Bromothiophene-3-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromo-functional group. The carboxylic acid moiety provides additional handle for derivatization via amide formation or esterification. Its bench-stable solid form and compatibility with standard reaction conditions make it a practical choice for constructing complex thiophene-based scaffolds in 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-H317-H319
|
|
|
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: