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 38275-43-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(Methylthio)pyrimidine-5-carbonitrile features a pyrimidine core bearing a methylthio group at the 2-position and a nitrile at the 5-position, offering a robust scaffold for medicinal chemistry. The electron-deficient pyrimidine ring pairs with the polarizable sulfur-containing substituent to enable diverse coupling reactions and enhance target binding affinity in kinase inhibitor design. This compound exhibits bench-stable handling characteristics and integrates readily into multi-step synthetic sequences under standard conditions.
2-(Methylthio)pyrimidine-5-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its methylthio and cyano groups offer orthogonal reactivity for nucleophilic substitution, transition-metal-catalyzed coupling, and heterocycle elaboration. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis and API development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: