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 126533-97-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Morpholinothiazole-4-carbaldehyde features a morpholino group attached to a thiazole ring, delivering enhanced solubility and electronic modulation. The aldehyde functionality enables direct coupling in condensation reactions, serving as a key scaffold for bioactive molecule synthesis. This compound exhibits bench-stable handling and compatibility with diverse reaction conditions.
2-Morpholinothiazole-4-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based scaffolds through standard functional group transformations. Its aldehyde functionality facilitates reductive amination, Grignard additions, and coupling reactions with nucleophiles, while the morpholino group enhances solubility and modulates electronic properties. The compound exhibits bench stability and compatibility with common protecting groups, supporting its use in multi-step syntheses of bioactive molecules.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H315-H319-H332-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: