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 86443-51-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-N-ethylpyrimidin-4-amine features a pyrimidine core bearing a chloro group at C2 and an ethylamino substituent at C4, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient pyrimidine serves as a key intermediate in medicinal chemistry, particularly for kinase inhibitor development and nucleoside analog synthesis. The molecule exhibits enhanced solubility and stability under standard reaction conditions, facilitating efficient coupling processes.
2-Chloro-N-ethylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the N-ethylamino functionality offers tunable basicity and solubility. This compound exhibits bench stability and compatibility with standard coupling protocols, making it well-suited for modular synthesis of kinase inhibitors and other bioactive heterocycles.
|
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: