Eriodictyol
Title: Eriodictyol
CAS Registry Number: 552-58-9
CAS Name: 2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one
Additional Names: 3¢,4¢,5,7-tetrahydroxyflavanone
Molecular Formula: C15H12O6
Molecular Weight: 288.25
Percent Composition: C 62.50%, H 4.20%, O 33.30%
Literature References: Isoln from Eriodictyon californicum (H. & A.) Greene, Hydrophyllaceae: Geissman, J. Am. Chem. Soc. 62, 3258 (1940); from lemon: Mager, Z. Physiol. Chem. 274, 109 (1942); Horowitz, J. Am. Chem. Soc. 79, 6561 (1957); US 2857318 (1958 to U.S. Dept. Agr.). Structure and synthesis: Reichel et al., Ann. 550, 146 (1942); Zemplén et al., Ber. 76B, 1112 (1943); Pew, J. Org. Chem. 27, 2935 (1962). Synthesis: G. Wurm, U. Geres, Arch. Pharm. 315, 183 (1982). See also Bioflavanoids.
Properties: Needles with 1½ H2O from dil alc, dec 257° (rapid heating). After drying in vacuo at 100° for 6 hours, dec 267°. uv max (alc): 290, 326 nm (log e 2.54, 2.16). Sparingly sol in boiling water, hot alcohol, ether, glacial acetic acid; sol in dil alkalies.
Absorption maximum: uv max (alc): 290, 326 nm (log e 2.54, 2.16)
 
Derivative Type: 7-L-Rhamnoside
Additional Names: Eriodictin
Molecular Formula: C21H22O10
Molecular Weight: 434.39
Percent Composition: C 58.06%, H 5.10%, O 36.83%
Literature References: Isoln from citrin: Bruckner, Szent-Györgyi, Nature 138, 1057 (1936). Structure: Mager, loc. cit.
Properties: Crystals from ethyl acetate, dec 184-186°. [a]D20 -51.5° (in pyridine). Sol in water, acetone, alcohol; practically insol in ether.
Optical Rotation: [a]D20 -51.5° (in pyridine)

Others monographs:
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ParethoxycaineButoxycaine2-Naphthol-3,6-disulfonic AcidEthyl Oenanthate
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