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 733039-20-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-chloro-N-cyclopentylpyrimidin-4-amine features a sterically hindered cyclopentyl group attached to the pyrimidine nitrogen, enhancing metabolic stability. The electron-deficient pyrimidine core supports efficient coupling in cross-coupling reactions. This bench-stable derivative enables rapid access to functionalized heterocycles in medicinal chemistry and materials synthesis.
5-Bromo-2-chloro-N-cyclopentylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its dual halogen functionality. The bromo and chloro groups offer orthogonal reactivity for sequential functionalization, while the N-cyclopentyl substituent enhances solubility and modulates electronic properties. Bench-stable and compatible with standard reaction conditions, it facilitates efficient synthesis of complex pyrimidine-based scaffolds used in kinase inhibitor development and other pharmaceutical applications.
|
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: