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 1809004-78-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate features a fused thienopyridine core with a bromine atom at the 4-position and an ethyl ester group at the 2-position. This electrophilic scaffold enables direct functionalization in cross-coupling reactions, serving as a key building block for bioactive heterocycles. The molecule exhibits excellent stability under standard conditions and facilitates efficient diversification in medicinal chemistry campaigns.
Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate serves as a versatile building block for the synthesis of thienopyridine-based heterocycles. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the ester group supports further functionalization. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex scaffolds relevant in medicinal chemistry and materials science.
|
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: