Home > Name List By 2 > 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4, 5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

CAS No 491-50-9 , 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,
5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

  • Name: 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,
    5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
  • Synonyms: Quercimeritroside; CHEBI:28529; Quercetin-7-O-glucoside; Quercimeritrin;2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,
    5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; Quercimeritrin (6CI,7CI,8CI); C.I. 75710;
  • CAS Registry Number:
  • Flash Point: 302.8°C
  • Boiling Point: 859.2°Cat760mmHg
  • Density: 1.809g/cm3
  • Refractive index: 1.774
  • Flash Point: 302.8°C
  • Molecular Weight: 464.3763
  • InchiKey: BBFYUPYFXSSMNV-HMGRVEAOSA-N
  • InChI: InChI=1S/C21H20O12/c22-6-13-15(26)17(28)19(30)21(33-13)31-8-4-11(25)14-
    12(5-8)32-20(18(29)16(14)27)7-1-2-9(23)10(24)3-7/h1-5,13,15,17,19,21-26,
    28-30H,6H2/t13-,15-,17+,19-,21-/m1/s1
  • Molecular Formula: C21H20O12
  • Molecular Structure:CAS No:491-50-9 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,<br />5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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491-50-9 4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-3,5-dihydroxy-

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491-50-9 Quercetin-7-glucoside

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References of 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,
5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Title: Quercimeritrin
CAS Registry Number: 491-50-9
CAS Name: 2-(3,4-Dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-3,5-dihydroxy-4H-1-benzopyran-4-one
Synonyms: quercetin-7-D-glucoside; 3,3¢,4¢,5,7-pentahydroxyflavone-7-D-glucoside
Molecular Formula: C21H20O12
Molecular Weight: 464.38
Percent Composition: C 54.31%, H 4.34%, O 41.34%
Literature References: Found in flowers of Gossypium herbaceum L., Malvaceae: Perkin, J. Chem. Soc. 95, 2181 (1909); from leaves of Chrysanthemum ségetum L. and C. coronarium L., Compositae: Geissman, Steelink, J. Org. Chem. 22, 946 (1957); Anyas, Steelink, Arch. Biochem. Biophys. 90, 63 (1960). In the mother liquor from quercimeritrin the glucosides gossypitrin and isoquercitrin, q.v., are also found. Structure: Attree, Perkin, J. Chem. Soc. 1927, 234; Rao, Seshadri, Proc. Indian Acad. Sci. 9A, 365 (1939), C.A. 34, 1071 (1940); Pacheco, Grouiller, Compt. Rend. 253, 1178 (1961).
 
Derivative Type: Trihydrate
Properties: Yellow plates from aq pyridine. The water of crystn is given up at 100°, the anhydr material is hygroscopic, mp 247-249°. uv max (ethanol): 372, 257 nm (log e 4.33, 4.38). Practically insol in cold water, more sol in hot water; sol in methanol. Sol in aq alkaline solns with deep yellow color. Is hydrolyzed by 7% H2SO4 yielding 1 mol quercetin and 1 mol D-glucose.
Melting point: mp 247-249°
Absorption maximum: uv max (ethanol): 372, 257 nm (log e 4.33, 4.38)
 
Derivative Type: Gossypitrin
Molecular Formula: C21H20O13
Molecular Weight: 480.38
Percent Composition: C 52.51%, H 4.20%, O 43.30%
Properties: Orange-yellow needles melting at 200-202°; slightly sol in alcohol and acetic acid.