ChemSpider 2D Image | 13a-Hydroxy-2,3-dimethoxy-6a,13a-dihydrochromeno[3,4-b]furo[3,2-g]chromen-13(6H)-one | C20H16O7

13a-Hydroxy-2,3-dimethoxy-6a,13a-dihydrochromeno[3,4-b]furo[3,2-g]chromen-13(6H)-one

  • Molecular FormulaC20H16O7
  • Average mass368.337 Da
  • Monoisotopic mass368.089600 Da
  • ChemSpider ID24842947

More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

13a-Hydroxy-2,3-dimethoxy-6a,13a-dihydrochromeno[3,4-b]furo[3,2-g]chromen-13(6H)-on [German] [ACD/IUPAC Name]
13a-Hydroxy-2,3-dimethoxy-6a,13a-dihydrochromeno[3,4-b]furo[3,2-g]chromen-13(6H)-one [ACD/IUPAC Name]
13a-Hydroxy-2,3-diméthoxy-6a,13a-dihydrochroméno[3,4-b]furo[3,2-g]chromén-13(6H)-one [French] [ACD/IUPAC Name]
Furo[3',2':6,7][1]benzopyrano[2,3-c][1]benzopyran-13(6H)-one, 6a,13a-dihydro-13a-hydroxy-2,3-dimethoxy- [ACD/Index Name]
12a-Hydroxyerosone
12α-Hydroxyerosone
13-hydroxy-16,17-dimethoxy-2,6,20-trioxapentacyclo[11.8.0.0??,????.0?,?.0???,???]henicosa-3(11),4,7,9,14,16,18-heptaen-12-one
13-hydroxy-16,17-dimethoxy-2,6,20-trioxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-3(11),4,7,9,14,16,18-heptaen-12-one
66322-32-5 [RN]
6a,13a-Dihydro-13a-hydroxy-2,3-dimethoxy[1]benzopyrano[3,4-b]furo[3,2-g][1]benzopyran-13(6H)-one, 9CI

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

Density: 1.5±0.1 g/cm3
Boiling Point: 581.5±50.0 °C at 760 mmHg
Vapour Pressure: 0.0±1.7 mmHg at 25°C
Enthalpy of Vaporization: 91.5±3.0 kJ/mol
Flash Point: 305.5±30.1 °C
Index of Refraction: 1.665
Molar Refractivity: 94.0±0.3 cm3
#H bond acceptors: 7
#H bond donors: 1
#Freely Rotating Bonds: 2
#Rule of 5 Violations: 0
ACD/LogP: 3.33
ACD/LogD (pH 5.5): 3.19
ACD/BCF (pH 5.5): 155.86
ACD/KOC (pH 5.5): 1291.73
ACD/LogD (pH 7.4): 3.19
ACD/BCF (pH 7.4): 155.67
ACD/KOC (pH 7.4): 1290.15
Polar Surface Area: 87 Å2
Polarizability: 37.3±0.5 10-24cm3
Surface Tension: 61.6±3.0 dyne/cm
Molar Volume: 253.3±3.0 cm3

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