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 479633-63-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine is a bench-stable heterocyclic scaffold featuring a chlorine atom at the 4-position and a tosyl group at the 7-position. This configuration enables selective coupling in late-stage functionalization, particularly in kinase inhibitor synthesis and transition-metal-catalyzed cross-coupling reactions. The electron-deficient pyrimidine core enhances reactivity under standard conditions.
4-Chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in the synthesis of purine-based scaffolds, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The tosyl group enhances solubility and stability, while the chloro substituent provides a reliable handle for nucleophilic substitution or transition-metal-mediated transformations. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry campaigns and process-scale 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: