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 149849-94-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-chloropyrimidine-4-carboxylate features a chlorinated pyrimidine core with a methyl ester at the C4 position, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient pyrimidine ring supports efficient nucleophilic substitution reactions, while the ester group facilitates downstream transformations. This bench-stable reagent delivers high functional group tolerance and is well-suited for medicinal chemistry applications requiring rapid access to substituted pyrimidines.
Methyl 2-chloropyrimidine-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient functionalization at the C2 position via nucleophilic substitution. Its chlorine atom exhibits high reactivity toward amines, thiols, and carbon nucleophiles under mild conditions, facilitating access to diverse pyrimidine derivatives. The ester group supports further transformations, including hydrolysis or reduction, enhancing its utility in medicinal chemistry and agrochemical research. Bench-stable and readily purified by flash chromatography, it integrates seamlessly into standard synthetic workflows.
|
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: