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2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate

group of stereoisomers with the chemical formula C₁₀H₁₂O₇
ChemicalSubstance group_of_stereoisomers Q104396302
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Summary

2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate is a group of stereoisomers[1].

Key Facts

  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's instance of is recorded as group of stereoisomers[2].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's CAS Registry Number is recorded as 87087-60-3[3].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's canonical SMILES is recorded as O=C(OCC(O)CO)C1=CC(O)=C(O)C(O)=C1[4].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's InChI is recorded as InChI=1S/C10H12O7/c11-3-6(12)4-17-10(16)5-1-7(13)9(15)8(14)2-5/h1-2,6,11-15H,3-4H2[5].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's InChIKey is recorded as PDEQYQCQYAQJPN-UHFFFAOYSA-N[6].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's chemical formula is recorded as C₁₀H₁₂O₇[7].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's subclass of is recorded as chemical compound[8].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's PubChem CID is recorded as 5317465[9].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's ChEBI ID is recorded as 168599[10].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's found in taxon is recorded as Rheum officinale[11].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's found in taxon is recorded as Lotus japonicus[12].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's Human Metabolome Database ID is recorded as HMDB0039177[13].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+244.05830272400001'}[14].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's SureChEMBL ID is recorded as 1392652[15].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's DSSTox substance ID is recorded as DTXSID901239764[16].
  • 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate's UniChem compound ID is recorded as 22983173[17].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Tannins and related compounds. X. Rhubarb (2): Isolation and structures of a glycerol gallate, gallic acid glucoside gallates, galloylglucoses and isolindleyin.. wikidata.org.
  11. [12] ↑ . Gallic acid esters of bergenin and norbergenin from Mallotus japonicus. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-3-dihydroxypropyl-3-4-5-trihydroxybenzoate
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BibTeX @misc{4ortxyz_2-3-dihydroxypropyl-3-4-5-trihydroxybenzoate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2,3-dihydroxypropyl 3,4,5-trihydroxybenzoate}}, year = {2026}, url = {https://4ort.xyz/entity/2-3-dihydroxypropyl-3-4-5-trihydroxybenzoate}, note = {Accessed: 2026-05-03}}
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