Nomenclature
CAS number: 301-19-9
3-[[6-
O-(6-Deoxy-α-
l-mannopyranosyl)-β-
d-galactopyranosyl]oxy]-7-[(6-deoxy-α-
l-mannopyranosyl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4
H-1-benzopyran-4-one; kaempferol 3-robinoside 7-rhamnoside.
C
33H
40O
19; mol wt 740.66.
C 53.51%, H 5.44%, O 41.04%.
Description and references
Dimorphic flavanoid isolated from the leaves
and flowers of Robinia pseudoacacia L., Leguminosae: C. Zwenger, F. Dronke, Ann. suppl. 1, 257 (1861); C. Sando, J. Biol. Chem. 94, 675 (1932). Structure:
Zemplén, Bognár, Ber. 74B, 1783 (1941). Total synthesis and structure: L. Farkas et
al., Phytochemistry 15, 215 (1976).
Derivative
β-Form.
Properties
Yellow crystals, mp 250-254° (Farkas); also reported as straw-yellow
needles from alc, mp 249-250° (Sando). uv max (ethanol): 352, 368 nm (log ε 4.14, 4.18), Jurd, Horowitz,
J. Org. Chem. 22, 1619 (1957). Sol in hot water, hot alc; practically insol in ether. On hydrolysis
yields
kaempferol,
q.v.Derivative
α-Form.
Properties
Obtained by crystallization from water and dehydrating, mp 195-197° (Sando).
Also reported as hydrate, yellow needles from aq methanol, mp 196-199° (Farkas).