Found 3 results

Search term: MF = 'C_{35}H_{32}O_{11}'
ChemSpider 2D Image | curtisian D | C35H32O11

curtisian D

  • Molecular FormulaC35H32O11
  • Average mass628.622 Da
  • Monoisotopic mass628.194458 Da
  • ChemSpider ID9939264

More details:

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

3-Hydroxybutanoate de 5',6'-diacétoxy-4,4''-dihydroxy-3'-[(3-phénylpropanoyl)oxy]-1,1':4',1''-terphényl-2'-yle [French] [ACD/IUPAC Name]
5',6'-Diacetoxy-4,4''-dihydroxy-3'-[(3-phenylpropanoyl)oxy]-1,1':4',1''-terphenyl-2'-yl 3-hydroxybutanoate [ACD/IUPAC Name]
5',6'-Diacetoxy-4,4''-dihydroxy-3'-[(3-phenylpropanoyl)oxy]-1,1':4',1''-terphenyl-2'-yl-3-hydroxybutanoat [German] [ACD/IUPAC Name]
Benzenepropanoic acid, 5',6'-bis(acetyloxy)-4,4''-dihydroxy-3'-(3-hydroxy-1-oxobutoxy)[1,1':4',1''-terphenyl]-2'-yl ester [ACD/Index Name]
curtisian D
5',6'-bis(acetyloxy)-4,4''-dihydroxy-3'-[(3-phenylpropanoyl)oxy]-1,1':4',1''-terphenyl-2'-yl 3-hydroxybutanoate
  • Miscellaneous

    • Chemical Class:

      A <ital>para</ital>-terphenyl that consists of 1,4-diphenylbenzene substituted by acetyloxy groups at positions 5' and 6', hydroxy groups at positions 4 and 4'', a (3-phenylpropanoyl)oxy group at posi tion 3' and a (3-hydroxybutanoyl)oxy group at position 2'. It is isolated from the fruit body of the mushroom <ital>Paxillus curtisii</ital> and exhibits radical scavenging activity ChEBI CHEBI:65699
      A para-terphenyl that consists of 1,4-diphenylbenzene substituted by acetyloxy groups at positions 5' and 6', hydroxy groups at positions 4 and 4'', a (3-phenylpropanoyl)oxy group at posi; tion 3' and a (3-hydroxybutanoyl)oxy group at position 2'. It is isolated from the fruit body of the mushroom Paxillus curtisii and exhibits radical scavenging activity ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:65699
      A para-terphenyl that consists of 1,4-diphenylbenzene substituted by acetyloxy groups at positions 5' and 6', hydroxy groups at positions 4 and 4'', a (3-phenylpropanoyl)oxy group at position 3' and a (3-hydroxybutanoyl)oxy group at position 2'. It is isolated from the fruit body of the mushroom Paxillus curtisii and exhibits radical scavenging activity ChEBI CHEBI:65699

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

Density: 1.3±0.1 g/cm3
Boiling Point: 849.3±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±3.3 mmHg at 25°C
Enthalpy of Vaporization: 129.3±3.0 kJ/mol
Flash Point: 269.7±27.8 °C
Index of Refraction: 1.608
Molar Refractivity: 164.4±0.3 cm3
#H bond acceptors: 11
#H bond donors: 3
#Freely Rotating Bonds: 15
#Rule of 5 Violations: 2
ACD/LogP: 2.81
ACD/LogD (pH 5.5): 4.23
ACD/BCF (pH 5.5): 969.24
ACD/KOC (pH 5.5): 4768.40
ACD/LogD (pH 7.4): 4.03
ACD/BCF (pH 7.4): 612.15
ACD/KOC (pH 7.4): 3011.63
Polar Surface Area: 166 Å2
Polarizability: 65.2±0.5 10-24cm3
Surface Tension: 55.1±3.0 dyne/cm
Molar Volume: 475.5±3.0 cm3

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