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 204319-69-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This trifluoromethylthiazole derivative features a reactive hydroxymethyl group positioned at the 4-position of a stable thiazole scaffold. The electron-withdrawing trifluoromethyl substituent enhances the electrophilicity of the adjacent carbon, enabling efficient coupling reactions in synthetic workflows. Designed for use in medicinal chemistry and functional materials synthesis, this compound offers improved solubility and stability under standard bench conditions.
(4-(Trifluoromethyl)thiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the efficient construction of thiazole-containing scaffolds via standard functional group transformations. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the pendant alcohol facilitates derivatization through esterification, etherification, or oxidation to aldehyde. The compound exhibits excellent bench stability and compatibility with common reaction conditions, making it a practical choice for modular 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 : H302-H319
|
|
|
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: