Jaceidin

Jaceidin
Names
	IUPAC name 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one
	Other names Jaceidine; Quercetagetin 3,3',6-trimethyl ether
Identifiers
CAS Number	10173-01-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	4576662 ;
PubChem CID	5464461;
CompTox Dashboard (EPA)	DTXSID30144148 ;
	InChI InChI=1S/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3 Key: XUWTZJRCCPNNJR-UHFFFAOYSA-N ; InChI=1/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3 Key: XUWTZJRCCPNNJR-UHFFFAOYAP;
	SMILES COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)OC)O;
Properties
Chemical formula	C18H16O8
Molar mass	360.31 g/mol
Melting point	130 - 135 °C
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Jaceidin is an O-methylated flavonol. It can be found in Chamomilla recutita,^[1] in Centaurea jacea and can be synthetized.^[2] Jaceidin has many different characteristics, such as a molar mass of 360.31 g/mol. It also has a melting point of 130 - 135 °C.^[3]

Glycosides

Jacein

References

^ Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert. Miroslav Repcák, Vanda Svehlíková, Ján Imrich and Kalevi Pihlaja, Biochemical Systematics and Ecology, Volume 27, Issue 7, October 1999, Pages 727-732
^ The synthesis of jaceidin. K. Fukui, T. Matsumoto, S. Nakamura, M. Nakayama and T. Horie, Cellular and Molecular Life Sciences, Volume 24, Number 2 / february 1968
^ Pubchem. "Jaceidin | C18H16O8 - PubChem". pubchem.ncbi.nlm.nih.gov. Retrieved 2017-03-09.

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[1] Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert. Miroslav Repcák, Vanda Svehlíková, Ján Imrich and Kalevi Pihlaja, Biochemical Systematics and Ecology, Volume 27, Issue 7, October 1999, Pages 727-732

[2] The synthesis of jaceidin. K. Fukui, T. Matsumoto, S. Nakamura, M. Nakayama and T. Horie, Cellular and Molecular Life Sciences, Volume 24, Number 2 / february 1968

[3] Pubchem. "Jaceidin | C18H16O8 - PubChem". pubchem.ncbi.nlm.nih.gov. Retrieved 2017-03-09.

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