Hexahydroxydiphenic acid

Hexahydroxydiphenic acid
Names

Preferred IUPAC name 4,4',5,5',6,6'-Hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylic acid
Other names HHDP 3,4,5,3',4',5'-Hexahydroxydiphenate 3,4,5,3',4',5'-Hexahydroxydiphenic acid
Identifiers
3D model (JSmol)	Interactive image
ChemSpider	8490515^N
PubChem CID	10315050
InChI InChI=1S/C14H10O10/c15-5-1-3(13(21)22)7(11(19)9(5)17)8-4(14(23)24)2-6(16)10(18)12(8)20/h1-2,15-20H,(H,21,22)(H,23,24)^N Key: MFTSECOLKFLUSD-UHFFFAOYSA-N^N InChI=1/C14H10O10/c15-5-1-3(13(21)22)7(11(19)9(5)17)8-4(14(23)24)2-6(16)10(18)12(8)20/h1-2,15-20H,(H,21,22)(H,23,24) Key: MFTSECOLKFLUSD-UHFFFAOYAZ
SMILES O=C(O)c2cc(O)c(O)c(O)c2c1c(O)c(O)c(O)cc1C(=O)O
Properties
Chemical formula	C₁₄H₁₀O₁₀
Molar mass	338.22 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Hexahydroxydiphenic acid is a component of some ellagitannins^[1] such as casuarictin. Luteic acid is the lactone and ellagic acid is the dilactone of hexahydroxydiphenic acid.

References

↑ Ellagitannin Chemistry. Studies on the Stability and Reactivity of 2,4-HHDP-Containing Glucopyranose Systems. Ken S. Feldman, Malliga R. Iyer and Yanze Liu, J. Org. Chem., 2003, 68 (19), pp. 7433–7438, doi:10.1021/jo034495x

Moieties

Lactones

Monomers

C-glycosidic ellagitannins

Dehydroellagitannins (molecules with
dehydrohexahydroxydiphenic acid (DHHDP)

Transformed ellagitannins

molecules with chebulic acid	Chebulagic acid Chebulinic acid
molecules with Elaeocarpusinic acid	Elaeocarpusin Helioscopin B Mallojaponin (1-O-Galloyl-2,4-elaeocarpusinoyl-3,6-(R)-valoneayl-beta-D-glucose)

Oligomers

Dimers: Agrimoniin; Cornusiin E (dimer of tellimagrandin II); Lambertianin A and B; Nobotanin B; Roburin A, B, C and D; Sanguiin H-6

Other

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