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 115581-36-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-5-(methylthio)pyrimidine serves as a pivotal heterocyclic scaffold in medicinal chemistry, integrating a reactive chlorine atom with a sulfur-tethered methyl group. This combination enables selective functionalization in cross-coupling reactions and facilitates the construction of complex pyrimidine-based pharmaceuticals under mild conditions. The molecule exhibits robust stability and favorable solubility profiles in common organic solvents.
2-Chloro-5-(methylthio)pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds through nucleophilic substitution. The chloro group at C2 facilitates coupling with amines, thiols, and other nucleophiles under mild conditions, while the methylthio substituent provides moderate electron donation and orthogonal reactivity. Its bench stability and compatibility with common reaction protocols make it well-suited for iterative synthesis campaigns in API development.
|
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: