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 930-96-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromothiophene-2-carboxaldehyde features a brominated thiophene ring fused to an aldehyde group, enabling direct functionalization in cross-coupling and heterocyclic synthesis. This electron-deficient scaffold facilitates rapid derivatization under standard conditions, delivering access to bioactive scaffolds and advanced materials.
3-Bromothiophene-2-carboxaldehyde serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions and functionalization at the bromine site. The aldehyde group facilitates nucleophilic additions, oxime formation, and condensation reactions, offering access to diverse pharmaceutical and agrochemical scaffolds. Its bench-stable nature and compatibility with common protecting groups make it well-suited for multi-step synthetic sequences in medicinal chemistry and process development 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: