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 17551-52-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Chloro-2-methylpyrimidin-4(1H)-one features a chlorine substituent at C6 and a methyl group at C2, creating a sterically hindered, electron-deficient pyrimidinone core. This structure enables efficient coupling in nucleophilic substitution reactions and serves as a key scaffold in medicinal chemistry for constructing bioactive heterocycles under mild conditions.
6-Chloro-2-methylpyrimidin-4(1H)-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the enolizable carbonyl and methyl substituent support diverse functionalization. The compound exhibits good bench stability and compatibility with standard coupling protocols, making it valuable for synthesizing heterocyclic intermediates and API candidates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H318
|
|
|
Precautionary Statements : P264-P270-P280-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: