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 43088-67-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-5-methylthieno[2,3-d]pyrimidine features a fused thienopyrimidine core with orthogonal electron-withdrawing and electron-donating substituents, enabling selective functionalization in medicinal chemistry. This scaffold exhibits enhanced metabolic stability and favorable solubility profiles under standard conditions, facilitating direct incorporation into kinase inhibitor and antiviral lead compounds.
4-Chloro-5-methylthieno[2,3-d]pyrimidine serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of biologically relevant scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the methyl substituent enhances solubility and modulates electronic properties. The fused thienopyrimidine core provides structural rigidity and metabolic stability, making it valuable in medicinal chemistry campaigns targeting kinase inhibitors and antiviral agents. Bench-stable and compatible with standard coupling protocols, it simplifies purification and scale-up 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: