3-(cis-5,6-Dihydroxycyclohexa-1,3-dien-1-yl)propanoic acid

3-(*cis*-5,6-Dihydroxycyclohexa-1,3-dienyl)propanic acid
Names
	IUPAC name 3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoic acid
	Systematic IUPAC name 3-[(5,6-Dihydroxycyclohexa-1,3-dien-1-yl)]propanoic acid
Identifiers
3D model (JSmol)	Anion: Interactive image; Acid: Interactive image;
ChEBI	Anion: CHEBI:60089; Acid: CHEBI:10472;
ChemSpider	Anion: 26331810; Acid: 391536;
KEGG	Acid: C11588;
PubChem CID	Anion: 46878520; Acid: 443290;
	InChI InChI=1S/C9H12O4/c10-7-3-1-2-6(9(7)13)4-5-8(11)12/h1-3,7,9-10,13H,4-5H2,(H,11,12)/p-1/t7-,9+/m0/s1 Key: RKDFGWAXBBGKMR-IONNQARKSA-M; Acid: InChI=1S/C9H12O4/c10-7-3-1-2-6(9(7)13)4-5-8(11)12/h1-3,7,9-10,13H,4-5H2,(H,11,12)/t7-,9+/m0/s1 Key: RKDFGWAXBBGKMR-IONNQARKSA-N;
	SMILES Anion: O=C([O-])CCC1=CC=C[C@H](O)[C@@H]1O; Acid: C1=C[C@@H]([C@@H](C(=C1)CCC(=O)O)O)O;
Properties
Chemical formula	C9H12O4
Molar mass	184.191 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

3-(cis-5,6-Dihydroxycyclohexa-1,3-dien-1-yl)propanoic acid^[1] is an chemical with the formula C₉H₁₂O₄. The conjugate base is 3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate.^[2]

It is a substrate of 3-(cis-5,6-dihydroxycyclohexa-1,3-dien-1-yl)propanoate dehydrogenase.^[3]

References

^ team, the MetaNetX. "MetaNetX: MNXM730695 - 3-(cis-5,6-dihydroxycyclohexa-1,3-dienyl)propanoate". MetaNetX. Retrieved 2026-03-12.
^ "Rhea - reaction knowledgebase". www.rhea-db.org. Archived from the original on 2026-01-17. Retrieved 2026-03-13.
^ Díaz, Eduardo; Ferrández, Abel; García, José L. (1998). "Characterization of the hca Cluster Encoding the Dioxygenolytic Pathway for Initial Catabolism of 3-Phenylpropionic Acid in Escherichia coli K-12". Journal of Bacteriology. 180 (11). American Society for Microbiology: 2915–2923. doi:10.1128/jb.180.11.2915-2923.1998. ISSN 0021-9193. PMC 107259. PMID 9603882.

[1] team, the MetaNetX. "MetaNetX: MNXM730695 - 3-(cis-5,6-dihydroxycyclohexa-1,3-dienyl)propanoate". MetaNetX. Retrieved 2026-03-12.

[2] "Rhea - reaction knowledgebase". www.rhea-db.org. Archived from the original on 2026-01-17. Retrieved 2026-03-13.

[3] Díaz, Eduardo; Ferrández, Abel; García, José L. (1998). "Characterization of the hca Cluster Encoding the Dioxygenolytic Pathway for Initial Catabolism of 3-Phenylpropionic Acid in Escherichia coli K-12". Journal of Bacteriology. 180 (11). American Society for Microbiology: 2915–2923. doi:10.1128/jb.180.11.2915-2923.1998. ISSN 0021-9193. PMC 107259. PMID 9603882.

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