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Viniferal

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Viniferal
Chemical structure of viniferal
Names
IUPAC name (2R,2′S,3R,3′S)-3′-(3,5-Dihydroxyphenyl)-6′-hydroxy-2,2′-bis(4-hydroxyphenyl)-2,2′,3,3′-tetrahydro--5-carbaldehyde
Other names (-)-Viniferal
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C35H26O8/c36-17-18-1-10-29-27(11-18)32(35(42-29)20-4-8-23(38)9-5-20)28-15-26(41)16-30-33(28)31(21-12-24(39)14-25(40)13-21)34(43-30)19-2-6-22(37)7-3-19/h1-17,31-32,34-35,37-41H/t31-,32-,34+,35-/m0/s1Key: DHTHKPNODOWMKF-VPIGGYNKSA-N
  • InChI=1/C35H26O8/c36-17-18-1-10-29-27(11-18)32(35(42-29)20-4-8-23(38)9-5-20)28-15-26(41)16-30-33(28)31(21-12-24(39)14-25(40)13-21)34(43-30)19-2-6-22(37)7-3-19/h1-17,31-32,34-35,37-41H/t31-,32-,34+,35-/m0/s1Key: DHTHKPNODOWMKF-VPIGGYNKBX
SMILES
  • O=CC1=CC=C(O(C2=CC=C(O)C=C2)3C4=CC(O)=CC5=C4(C6=CC(O)=CC(O)=C6)(C7=CC=C(O)C=C7)O5)C3=C1
Properties
Chemical formula C35H26O8
Molar mass 574.585 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Viniferal is a hydroxystilbenoid with an aldehyde group found in Vitis vinifera (grapevine).

References

  1. Ito, J (1996). "Absolute structures of new hydroxystilbenoids, vitisin C and viniferal, from Vitis vinifera 'Kyohou'". Tetrahedron. 52 (30): 9991. doi:10.1016/0040-4020(96)00543-1.

External links

Type of stilbenoids (molecules with a C6-C2-C6 backbone)
Types

Template:Natural-phenol-stub

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