Cas no 15222-53-4 (9H-Xanthen-9-one,1-hydroxy-3,6-dimethoxy-8-methyl-)
15222-53-4 structure
Product Name:9H-Xanthen-9-one,1-hydroxy-3,6-dimethoxy-8-methyl-
CAS No:15222-53-4
MF:C16H14O5
MW:286.279365062714
CID:158927
PubChem ID:5358904
Update Time:2025-04-19
9H-Xanthen-9-one,1-hydroxy-3,6-dimethoxy-8-methyl- Chemical and Physical Properties
Names and Identifiers
-
- 1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one
- 1-hydroxy-3,6-dimethoxy-8-methylxanthen-9-one
- 9H-Xanthen-9-one,1-hydroxy-3,6-dimethoxy-8-methyl-
- 1-hydroxy-3,6-dimethoxy-8-methyl-xanthen-9-one
- 1-hydroxy-3,6-dimethoxy-8-methylxanthone
- AC1NSDCX
- CHEBI:67821
- CHEMBL470650
- DivK1c_006167
- lichenxanthone
- Lichexanthone
- lichixanthone
- SpecPlus_000071
- Spectrum5_001811
- SureCN4272316
- 15222-53-4
- NS00134237
- 9H-Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl- (9CI)
- 9H-Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl-
- NSC288657
- KBio1_001111
- NSC-288657
- Xanthen-9-one,6-dimethoxy-8-methyl-
- 1-Hydroxy-3,6-dimethoxy-8-methyl-9H-xanthen-9-one #
- QDLAGTHXVHQKRE-UHFFFAOYSA-N
- NSC 288657
- LICHEXANTHONE B804322K045
- DTXSID80164977
- 9H-Xanthen-9-one,6-dimethoxy-8-methyl-
- 92O5D9Z07W
- Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl-
- SCHEMBL4272316
- Q27136297
- UNII-92O5D9Z07W
- ConMedNP.1983
-
- Inchi： 1S/C16H14O5/c1-8-4-9(19-2)6-12-14(8)16(18)15-11(17)5-10(20-3)7-13(15)21-12/h4-7,17H,1-3H3
- InChI Key： QDLAGTHXVHQKRE-UHFFFAOYSA-N
- SMILES： O1C2C=C(C=C(C=2C(C2C(C)=CC(=CC1=2)OC)=O)O)OC
Computed Properties
- Exact Mass: 286.08412
- Monoisotopic Mass: 286.08412354g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 21
- Rotatable Bond Count: 2
- Complexity: 398
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.5
- Topological Polar Surface Area: 65?2
Experimental Properties
- PSA: 64.99
9H-Xanthen-9-one,1-hydroxy-3,6-dimethoxy-8-methyl- Related Literature
-
Fidele Ntie-Kang,Lydia L. Lifongo,Conrad V. Simoben,Smith B. Babiaka,Wolfgang Sippl,Luc Meva'a Mbaze RSC Adv. 2014 4 28728
-
2. Biogenetic-type synthesis of heptaketide natural products: alternariol and lichexanthoneJ. V. Hay,T. M. Harris J. Chem. Soc. Chem. Commun. 1972 953b
-
Mark J. Calcott,David F. Ackerley,Allison Knight,Robert A. Keyzers,Jeremy G. Owen Chem. Soc. Rev. 2018 47 1730
-
Laura P. Ióca,Pierre-Marie Allard,Roberto G. S. Berlinck Nat. Prod. Rep. 2014 31 646
-
Khanh-Hung Nguyen,Marylène Chollet-Krugler,Nicolas Gouault,Sophie Tomasi Nat. Prod. Rep. 2013 30 1490
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