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Methyl dichloroasterrate
SpectraBase Compound ID A4ZdJzcKTFx
InChI InChI=1S/C18H16Cl2O8/c1-7-12(19)14(22)11(18(24)27-4)16(13(7)20)28-15-9(17(23)26-3)5-8(21)6-10(15)25-2/h5-6,21-22H,1-4H3
InChIKey UWTOESDPWKUNBD-UHFFFAOYSA-N
Mol Weight 431.22 g/mol
Molecular Formula C18H16Cl2O8
Exact Mass 430.022223 g/mol
Copyright Copyright © 2024-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-65-9-5
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • METHYL-3,5-DICHLOROASTERRIC-ACID
  • 3,5-Dichloro-2-hydroxy-6-(4-hydroxy-2-methoxy-6-methoxycarbonylphenoxy)-4-methylbenzoic acid methyl ester
  • Methyl 3,5-bis(chloranyl)-2-(2-methoxy-6-methoxycarbonyl-4-oxidanyl-phenoxy)-4-methyl-6-oxidanyl-benzoate
  • Methyl 3,5-dichloro-2-hydroxy-6-(4-hydroxy-2-methoxy-6-methoxycarbonyl-phenoxy)-4-methyl-benzoate
Title Journal or Book Year
Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs. The Journal of Antibiotics 2002
New Chlorinated Diphenyl Ethers from an Aspergillus Species Journal of Natural Products 2001

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