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Maleic Anhydride And Anthracene Product

Anthracene-maleic anhydride Diels-Alder adduct

  • Formula: CxviiiH12O3
  • Molecular weight: 276.2861
  • IUPAC Standard InChI: InChI=1S/C18H12O3/c19-17-15-13-9-v-ane-2-6-10(9)14(16(fifteen)18(20)21-17)12-8-4-3-7-11(12)13/h1-8,13-16H

    InChI version 1.06

  • IUPAC Standard InChIKey: PSKVQQJLLWSBFV-UHFFFAOYSA-N
  • CAS Registry Number: 5443-sixteen-3
  • Chemic construction: C18H12O3
    This construction is as well available as a 2d Mol file or equally a computed 3d SD file
    The 3d structure may be viewed using Java or Javascript.
  • Other names: Anthracene, 2,v-furandione adduct; Anthracene,maleic anhydride adduct; endo-9,ten-(α,β-Succinic anhydride)anthracene; 9,x(three',4')-Furanoanthracene-12,14-dione; ix,ten-Dihydroanthraceno-9,ten-endo-α,β-succinic anhydride; 9,ten-Ethanoanthracene-11,12-dicarboxylic anhydride
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  • Information on this folio:
    • Reaction thermochemistry data
    • Mass spectrum (electron ionization)
    • References
    • Notes
  • Other information available:
    • Condensed stage thermochemistry information
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Reaction thermochemistry information

Go To: Top, Mass spectrum (electron ionization), References, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.s.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search class is also bachelor. Hereafter versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

Maleic anhydride  + Anthracene = Anthracene-maleic anhydride Diels-Alder adduct

By formula: C4H2Othree  + C14Hx = CeighteenH12O3

Quantity Value Units Method Reference Annotate
Δr -93. ± 2. kJ/mol Cm Kiselev, Mavrin, et al., 1982 liquid phase; solvent: Benzene
Δr -93.7 kJ/mol Eqk Lenz, Hegedus, et al., 1982 liquid phase; solvent: i,2,4-C6H3Cl3

Mass spectrum (electron ionization)

Go To: Top, Reaction thermochemistry information, References, Notes

Data compilation copyright past the U.S. Secretary of Commerce on behalf of the The statesA. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Heart, William Due east. Wallace, director

Spectrum

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Mass spectrum

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Origin Chemical Concepts
NIST MS number 155510

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References

Become To: Top, Reaction thermochemistry information, Mass spectrum (electron ionization), Notes

Data compilation copyright past the U.S. Secretary of Commerce on behalf of the U.s.a.A. All rights reserved.

Kiselev, Mavrin, et al., 1982
Kiselev, V.D.; Mavrin, G.5.; Konovalov, A.I., Thermodynamic principles of the occurrence of a Diels-Alder reaction in the presence of a Lewis acrid, Zh. Org. Khim., 1982, 18, 2505-2510. [all information]

Lenz, Hegedus, et al., 1982
Lenz, T.G.; Hegedus, 50.S.; Vaughan, J.D., Liquid stage thermochemical energy conversion systems - an application of Diels-Alder chemical science, Int. J. Energy Res., 1982, half dozen, 357-365. [all information]


Notes

Go To: Top, Reaction thermochemistry data, Mass spectrum (electron ionization), References

  • Symbols used in this document:
    Δr Enthalpy of reaction at standard conditions
  • Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
  • The National Institute of Standards and Engineering (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data independent therein have been selected on the basis of audio scientific judgment. However, NIST makes no warranties to that upshot, and NIST shall not be liable for whatsoever harm that may upshot from errors or omissions in the Database.
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Maleic Anhydride And Anthracene Product,

Source: https://webbook.nist.gov/cgi/cbook.cgi?ID=C5443163&Mask=608

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