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 1122-74-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Iodo-2-(methylthio)pyrimidine serves as a pivotal building block in heterocyclic synthesis, featuring a reactive iodine handle for palladium-catalyzed cross-coupling and a methylthio group that enables selective functionalization. This combination delivers high chemoselectivity under standard conditions, facilitating efficient access to complex pyrimidine derivatives used in medicinal chemistry and agrochemical development.
4-Iodo-2-(methylthio)pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable iodide leaving group. The methylthio substituent provides orthogonal reactivity and enhances solubility in organic media. This compound facilitates the construction of substituted pyrimidines relevant to medicinal chemistry and agrochemical scaffolds, with excellent bench stability and straightforward purification by flash chromatography or recrystallization.
|
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: