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 163165-92-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This oxazolylphenol integrates a sterically protected oxazole ring with a phenolic hydroxyl, enabling stable coupling in late-stage functionalization. The dihydrooxazole moiety enhances solubility and metabolic stability, while the para-phenylmethyl group confers rigidity and electron-rich character. This scaffold facilitates direct C–H arylation and serves as a key building block in bioactive heterocycle synthesis.
2-[(4S)-4,5-Dihydro-4-(phenylmethyl)-2-oxazolyl]phenol serves as a versatile chiral building block in synthetic medicinal chemistry, enabling access to oxazoline-containing scaffolds via standard coupling and cyclization protocols. Its bench-stable nature, functional group tolerance, and defined stereochemistry facilitate reliable incorporation into complex heterocyclic systems. The molecule functions effectively in transition-metal-catalyzed transformations and provides orthogonal reactivity for downstream derivatization in API synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: