Tropic acid
Names | |
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Preferred IUPAC name
3-Hydroxy-2-phenylpropanoic acid | |
Other names
2-Phenylhydracrylic acid; Tropate
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.008.201 |
EC Number |
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KEGG | |
MeSH | C011377 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C9H10O3 | |
Molar mass | 166.176 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
what is ?) | (|
Infobox references | |
Tropic acid is a chemical with IUPAC name 3-hydroxy-2-phenylpropanoic acid and condensed structural formula HOCH2CHPhCOOH. It is a laboratory reagent used in the chemical synthesis of atropine and hyoscyamine. Tropic acid is a chiral substance, existing as either a racemic mixture or as a single enantiomer.
Synthesis[]
Tropic acid synthesis 1:[1] | Tropic acid synthesis 2:[1] |
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References[]
- ^ a b Gadzikowska, M; Grynkiewicz, G (2002). "Tropane alkaloical and phytochemical analysis". Acta Poloniae Pharmaceutica. 59 (2): 149–60. PMID 12365608.
- ^ Sletzinger, Paulsen, U.S. Patent 2,390,278 (1945 to Merck & Co.).
- ^ Blicke, U.S. Patent 2,716,650 (1955 to University of Michigan).
- ^ DE 923426, Blicke, Frederick Franklin, "Verfahren zur Herstellung von α-substituierten β-Oxypropionsäuren [Process for the preparation of α-substituted β-oxypropionic acids]", published 1955-02-14, assigned to Sterling Drug Inc.
Categories:
- Beta hydroxy acids
- Propionic acids
- Organic compound stubs