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 62802-43-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-N,N-dimethylpyrimidin-5-amine features a chlorinated pyrimidine core with a dimethylamino group at the 5-position, enabling efficient coupling in nucleophilic substitution reactions. This bench-stable reagent integrates readily into heterocyclic scaffolds, offering high reactivity under mild conditions for synthetic and medicinal chemistry applications.
2-Chloro-N,N-dimethylpyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions with amines, alcohols, and thiols under mild conditions. The N,N-dimethylamino substituent enhances solubility and provides a handle for further derivatization. Bench-stable and readily purified by recrystallization or chromatography, it functions reliably in standard coupling protocols and is well-suited for scalable synthesis of heterocyclic intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H228
|
|
|
Precautionary Statements : P210-P240-P241-P280-P370+P378
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: