| Weight | 186.594 g/mol |
|---|---|
| Formula | C8H7ClO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2-Chloromandelic acid (10421-85-9)
o-chloromandelic acid
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- Enzymatic Hydrocyanation of a Sterically Hindered Aldehyde. Optimization of a Chemoenzymatic Procedure for (R)-2-Chloromandelic Acid (Organic Process Research & Development, 2003)
- Efficient production of (R)-o-chloromandelic acid by deracemization of o-chloromandelonitrile with a new nitrilase mined from Labrenzia aggregata (Applied Microbiology and Biotechnology, 2012)
- The Phase Behavior and Crystallization of 2-Chloromandelic Acid: The Crystal Structure of the Pure Enantiomer and the Behavior of Its Metastable Conglomerate (Crystal Growth & Design, 2011)
- Crystallization of the Racemic Compound and Conglomerate of (RS)-2-Chloromandelic Acid (Crystal Growth & Design, 2010)
- Identification and Characterization of Solid-State Nature of 2-Chloromandelic Acid (Journal of Pharmaceutical Sciences, 2009)
- Efficient Production of (R)-o-Chloromandelic Acid by Recombinant Escherichia coli Cells Harboring Nitrilase from Burkholderia cenocepacia J2315 (Organic Process Research & Development, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-chloromandelic acid
-
SMILESC1=CC=C(C(=C1)C(C(=O)O)O)Cl
-
InChIKeyRWOLDZZTBNYTMS-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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2-Chloromandelic acid
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