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 73664-43-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Iodo-N,N-dimethylacetamide delivers a highly reactive iodide handle for late-stage functionalization, enabling efficient coupling under mild conditions. This bench-stable acylating agent features a sterically protected dimethylamino group and an electron-deficient iodine site, facilitating selective transformations in complex molecular architectures.
2-Iodo-N,N-dimethylacetamide serves as a versatile iododomain reagent for late-stage functionalization, enabling efficient palladium-catalyzed cross-coupling reactions with arylborons and other nucleophiles. Its stable N,N-dimethyl amide group provides excellent functional group tolerance, while the iodine moiety facilitates reliable C–C bond formation under standard conditions. The compound exhibits bench stability, ease of handling, and straightforward purification, making it well-suited for synthetic applications in medicinal chemistry and process development.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 1760
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: