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 56012-38-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable thiazole derivative features a methyl-substituted heterocyclic core paired with a reactive hydroxymethyl group. The para-positioned methanol functionality enables straightforward derivatization in synthetic transformations, while the electron-rich thiazole ring enhances stability and solubility in polar organic solvents. Ideal for building complex heterocyclic scaffolds in medicinal chemistry applications.
(2-Methylthiazol-5-yl)methanol serves as a versatile building block for thiazole-based scaffolds in medicinal chemistry and materials science. Its benzylic alcohol functionality enables direct functionalization via oxidation, protection, or coupling reactions. The molecule exhibits good bench stability and compatibility with standard synthetic protocols, facilitating efficient incorporation into complex heterocyclic architectures and enabling access to diverse bioactive analogs through well-established transformations.
|
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: