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 73418-86-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Ethoxypyrimidin-5-amine features a pyrimidine core functionalized with an ethoxy group at C2 and a primary amine at C5, enabling integration into heterocyclic scaffolds. This bench-stable derivative serves as a key building block for medicinal chemistry campaigns targeting kinase inhibitors and antiviral agents, where its electron-rich nitrogen atoms facilitate hydrogen bonding in target binding pockets.
2-Ethoxypyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its ethoxy group facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the primary amine supports derivatization via acylation or reductive alkylation. The compound exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis workflows 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: