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 197846-05-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromofuran-3-carboxylic acid features a brominated furan ring fused to a carboxylic acid group, enabling direct functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and agrochemical building blocks under standard conditions. The pendant acid facilitates derivatization via amide or ester formation, while the bromine serves as a handle for palladium-catalyzed cross-coupling reactions. Bench-stable and moisture-tolerant, it streamlines access to complex bioactive architectures.
2-Bromofuran-3-carboxylic acid serves as a versatile building block for the synthesis of brominated heterocycles and pharmaceutical intermediates. Its functionality enables direct coupling reactions, including Suzuki-Miyaura and Stille transformations, due to the stable bromo substituent. The carboxylic acid group facilitates derivatization via esterification or amidation, enhancing solubility and reactivity in synthetic sequences. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring orthogonal functional group handling.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: