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 776-53-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 4-amino-2-(methylthio)pyrimidin-5-carboxylate features a pyrimidine core functionalized with an amino group at C4, a methylthio substituent at C2, and an ethyl ester at C5. This combination enables direct incorporation into heterocyclic scaffolds via coupling reactions. The molecule exhibits enhanced solubility in common organic solvents and stability under standard bench conditions, facilitating use in synthetic medicinal chemistry workflows.
Ethyl 4-amino-2-(methylthio)pyrimidin-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its amino and methylthio groups offer orthogonal reactivity for selective functionalization, while the ester moiety facilitates downstream transformations. Bench-stable and readily purified, it functions effectively in coupling reactions, nucleophilic substitutions, and transition-metal-catalyzed processes common in medicinal chemistry 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: