3,4′-Dihydroxystilbene

3,4′-Dihydroxystilbene
Names

IUPAC name 3-[2-(4-hydroxyphenyl)ethenyl]phenol
Identifiers
3D model (Jmol)	(trans): Interactive image
ChemSpider	8346853 (trans)
PubChem	54350316 10171348 (trans)
InChI (trans): InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H/b5-4+ Key: UFGKEFGYNRJIGO-SNAWJCMRSA-N InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H Key: UFGKEFGYNRJIGO-UHFFFAOYSA-N (trans): InChI=1/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H/b5-4+ Key: UFGKEFGYNRJIGO-SNAWJCMRBG
SMILES (trans): Oc2cc(/C=C/c1ccc(O)cc1)ccc2
Properties
Chemical formula	C₁₄H₁₂O₂
Molar mass	212.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

3,4′-Dihydroxystilbene is a stilbenoid found in the roots of Hydrangea macrophylla.^[1]

References

↑ Lunularic acid and related compounds in liverworts, algae and Hydrangea. John Gorham, Phytochemistry, 1977, Volume 16, Issue 2, Pages 249–253, doi:10.1016/S0031-9422(00)86795-3

Hydroxystilbenes and their glycosides (monomeric forms)

Dihydroxylated

Trihydroxylated

Tetrahydroxylated

O-methylated

4-Methoxyresveratrol Gnetucleistol D (2-methoxyoxyresveratrol) Gnetucleistol E (3-methoxy-isorhapontigenin) Isorhapontigenin (3,4',5-trihydroxy-3'-methoxystilbene) Pinostilbene (3-methoxyresveratrol) Pterostilbene (3',5'-dimethoxyresveratrol) Rhapontigenin (piceatannol 4'-methyl ether)

Combretastatins	Combretastatin A-1 Combretastatin A-4

carboxylated

other acylations

of resveratrol	Piceid (trans-Resveratrol-3-O-glucoside) trans-Resveratrol-3-O-glucuronide Resveratroloside (trans-resveratrol-4'-O-beta-D-glucopyranoside)

of rhapontigenin	Rhapontigenin 3-O-rutinoside 4'-Methoxy-(E)-resveratrol 3-O-rutinoside Rhaponticin (Rhapontigenin glucoside)

Oligomeric forms

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