Journal of Pharmaceutical Sciences 2009-05-01

Identification and characterization of solid-state nature of 2-chloromandelic acid.

Quan He, Jesse Zhu, Hassan Gomaa, Michael Jennings, Sohrab Rohani

Index: J. Pharm. Sci. 98(5) , 1835-44, (2009)

Full Text: HTML

Abstract

The racemate and enantiomers of 2-chloromandelic acid were characterized by SS-NMR, XRPD, and FTIR. The binary melting point phase diagram was constructed by DSC (differential scanning calorimetry). The solid-state nature of 2-chloromandelic acid was identified to be a racemic compound. The crystal structure of racemic compound was determined to be monoclinic P2(1)/c.


Related Compounds

Related Articles:

QSAR-based solubility model for drug-like compounds.

2010-10-01

[Bioorg. Med. Chem. 18 , 7078-84, (2010)]

Modeling the retention mechanism for high-performance liquid chromatography with a chiral ligand mobile phase and enantioseparation of mandelic acid derivatives.

2015-06-01

[J. Sep. Sci. 38 , 2085-92, (2015)]

Resolution of 2-chloromandelic acid with (R)-(+)-N-benzyl-1-phenylethylamine: chiral discrimination mechanism.

2012-05-01

[Chirality 24(5) , 349-55, (2012)]

More Articles...