Nomenclature
CAS number: 569-77-7
2,3,4,6-Tetrahydroxy-5
H-benzocyclohepten-5-one.
C
11H
8O
5; mol wt 220.18.
C 60.00%, H 3.66%, O 36.33%.
Description and references
The aglycone of several glycosides from various
nutgalls. Prepn by oxidation of pyrogallol: Perkin, Steven, J. Chem. Soc. 83, 192 (1903);
Perkin, ibid. 101, 803
(1912); Nierenstein, Spiers, Ber. 46, 3151 (1913); Evans, Dehn, J. Am. Chem. Soc. 52, 3647 (1930). Structure:
Willst"atter, Heiss, Ann. 433, 17 (1923); Barltrop, Nicholson, J. Chem. Soc. 1948, 116. Synthesis: Caunt et al., ibid. 1950, 1631; 1951, 1313.
Properties
Deep red needles from glacial acetic acid, dec
274-275°. Sparingly sol in most solvents.Derivative
Diglucoside.
Nomenclature
Dryophantin. C
23H
28O
15; mol wt 544.46.
C 50.74%, H 5.18%, O 44.08%.
Properties
Coloring matter of “red pea” gall produced by Dryophanta divisa Ald. on Quercus pedunculata Ehrh., Fagaceae: Nierenstein, J. Chem. Soc. 115, 1328 (1919); Nierenstein, Swanton, Biochem. J. 38, 373 (1944). Dark
red needles with bronze luster, mp 220-221°. Slightly sol in water, cold alcohol; sol in
boiling alcohol; in methanol, acetone.Use
As an additive to edible or inedible fats or oils,
hydrocarbon fuels or lubricants, retards oxidation or metal contamination:
Thompson,
US 2770545 (1956 to Universal Oil Prod.).