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 51628-12-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(4-Iodophenyl)acetonitrile features a para-iodinated phenyl ring linked to a nitrile-bearing acetyl side chain, enabling direct incorporation into Suzuki-Miyaura and other cross-coupling reactions. The iodine moiety facilitates efficient palladium-catalyzed transformations, while the nitrile group offers synthetic versatility for downstream functionalization. This bench-stable reagent serves as a key building block in pharmaceutical and agrochemical synthesis.
2-(4-Iodophenyl)acetonitrile serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki and Sonogashira reactions due to its stable iodide functionality and compatible nitrile group. Its bench-stable nature and straightforward purification facilitate integration into multi-step syntheses of functionalized biaryls and heterocyclic scaffolds common in medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 3439
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302+H312-H331
|
|
|
Precautionary Statements : P261-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: