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 7336-51-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Acetamido-4-methylthiazole features a thiazole core functionalized with an acetamido group at the 2-position and a methyl substituent at the 4-position, delivering enhanced solubility and stability under standard conditions. This scaffold serves as a key building block in medicinal chemistry for accessing bioactive heterocycles.
2-Acetamido-4-methylthiazole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to thiazole-based scaffolds. Its acetamido group offers a handle for further functionalization, while the methyl substituent enhances stability and modulates reactivity. The compound exhibits excellent bench stability, facilitates straightforward purification, and participates reliably in standard coupling and cyclization protocols, making it well-suited for the synthesis of bioactive molecules and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: