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 2689-65-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Iodo-2-furaldehyde delivers a reactive aldehyde group flanked by an iodine-substituted furan ring, enabling direct coupling in cross-coupling and bioconjugation workflows. This bench-stable, moisture-tolerant reagent integrates efficiently into complex molecular architectures where halogenated heterocycles are required.
5-Iodo-2-furaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to iodinated furan-based scaffolds. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the iodine substituent supports palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and is readily purified by flash chromatography, making it well-suited for iterative synthetic sequences 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 : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: