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 182415-24-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-(Thiophen-2-yl)-1H-pyrazole-5-carboxylic acid features a fused heterocyclic core integrating a thiophene ring with a pyrazole scaffold, delivering enhanced electronic conjugation and planarity. This structure supports efficient coupling in medicinal chemistry applications, particularly as a building block for bioactive compounds targeting kinase pathways and receptor modulation. The carboxylic acid moiety enables direct derivatization via amide or ester formation under standard conditions.
3-(Thiophen-2-yl)-1H-pyrazole-5-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its pyrazole core provides structural rigidity and hydrogen-bonding capacity, while the thiophene moiety enhances π-conjugation and electronic properties. The carboxylic acid group enables direct derivatization via amide coupling, esterification, or salt formation, facilitating downstream functionalization in peptide mimetics, kinase inhibitors, and organic semiconductors. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: