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 6214-46-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-(4-hydroxypyrimidin-5-yl)acetate features a pyrimidine core functionalized with a hydroxyl group and an acetyl ester side chain, enabling direct incorporation into heterocyclic synthesis. This bench-stable intermediate supports efficient derivatization in medicinal chemistry workflows, particularly for nucleoside analogs and kinase inhibitors.
Ethyl 2-(4-hydroxypyrimidin-5-yl)acetate serves as a versatile building block for pyrimidine-based heterocycles, enabling straightforward functionalization at the C5 position. The pendant hydroxyl group facilitates derivatization via esterification or ether formation, while the ethyl acrylate moiety supports palladium-catalyzed cross-coupling reactions. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step synthesis of kinase inhibitors and other medicinal chemistry scaffolds.
|
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: