For research use only. Not for therapeutic Use.
<span style="font-size:12px;"><span style="font-family:arial,helvetica,sans-serif;">3-(4-Chlorophenyl)glutaramic Acid (CAS 1141-23-7) can be used as dendritic ester raw material for organic synthesis or pharmaceutical intermediate and synthesis. </span></span>
Catalog Number | R034755 |
CAS Number | 1141-23-7 |
Synonyms | β-(2-Amino-2-oxoethyl)-4-chloro-benzenepropanoic Acid; 3-(p-Chlorophenyl)glutaramic Acid |
Molecular Formula | C11H12ClNO3 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 5-amino-3-(4-chlorophenyl)-5-oxopentanoic acid |
InChI | InChI=1S/C11H12ClNO3/c12-9-3-1-7(2-4-9)8(5-10(13)14)6-11(15)16/h1-4,8H,5-6H2,(H2,13,14)(H,15,16) |
InChIKey | NLCJVRPOYTZTMS-UHFFFAOYSA-N |
SMILES | C1=CC(=CC=C1C(CC(=O)N)CC(=O)O)Cl |
Reference | <span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Jane, David E., et al. "Diastereoselective synthesis of all four isomers of 3-(4-chlorophenyl) glutamic acid: identification of the isomers responsible for the potentiation of L-homocysteic acid-evoked depolarizations in neonatal rat motoneurons." </span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of medicinal chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;"> 39.24 (1996): 4738-4743.<br /> |