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 33173-31-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-2-Acetoxy-3-phenylpropanoic acid features a chiral center at the 2-position, delivering enantioselective reactivity in synthetic transformations. The acetoxy group enables facile ester cleavage under mild conditions, while the phenyl substituent imparts rigidity and enhanced solubility in organic media. This configuration supports efficient incorporation into complex molecular architectures, particularly in medicinal chemistry applications requiring stereocontrol.
(S)-2-Acetoxy-3-phenylpropanoic acid serves as a versatile chiral building block for the synthesis of pharmaceutically relevant β-aryl-α-hydroxy acid motifs. Its acetoxy group enables facile deacetylation or participation in neighboring-group-assisted transformations, while the phenyl and carboxylic acid functionalities support orthogonal functionalization. The stereochemical integrity at C2 ensures reliable asymmetric synthesis outcomes, making it suitable for scale-up in medicinal chemistry campaigns requiring high enantiomeric purity and bench-stable handling.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: