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Reboul, J. P.; Oddon, Y.; Caranoni, C.; Soyfer, J. C.; Barbe, J.; Pèpe, G. (1987). "Structure du
Dihydro-9,10 Anthracène. Support Tricyclique de Médicaments Psychotropes".
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for the 9- and 10- carbon–hydrogen bonds are estimated at 78 kcal mol. Thus these bonds are about 20% weaker than typical C–H bonds.
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395:. Several isomers of dihydroanthracene are known, but the 9,10 derivative is most common. It is a colourless solid that is used as a carrier of H
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at the 9- and 10- positions. It is produced in the laboratory by dissolving metal reduction using sodium/
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is not compromised for the flanking rings, anthracene is susceptible to
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InChI=1S/C14H12/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-8H,9-10H2
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Collin, Gerd; Höke, Hartmut; Talbiersky, Jörg (2006). "Anthracene".
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Except where otherwise noted, data are given for materials in their
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108 to 109 °C (226 to 228 °F; 381 to 382 K)
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549:Bass, K. C. (1962). "9,10-Dihydroanthracene".
513:Ullmann's Encyclopedia of Industrial Chemistry
458: — analogue with three phenyl rings
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356:312 °C (594 °F; 585 K)
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252:Key: WPDAVTSOEQEGMS-UHFFFAOYSA-N
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390:polycyclic aromatic hydrocarbon
366:(at 25 °C , 100 kPa).
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444:bond dissociation energy
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28:9,10-Dihydroanthracene
382:9,10-Dihydroanthracene
273:c1ccc2c(c1)Cc3ccccc3C2
61:9,10-Dihydroanthracene
336:1.19 g mL
57:Preferred IUPAC name
489:1987AcCrC..43..537R
318: g·mol
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433:aluminium chloride
370:Infobox references
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552:Organic Syntheses
378:Chemical compound
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205:CompTox Dashboard
109:Interactive image
18:Dihydroanthracene
16:(Redirected from
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411:Because the
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326:White solid
68:Identifiers
584:Anthracenes
413:aromaticity
407:Preparation
323:Appearance
282:Properties
147:100.009.398
463:References
456:Triptycene
393:anthracene
311:Molar mass
193:Z142C238GB
120:ChemSpider
96:3D model (
75:CAS Number
518:Wiley-VCH
578:Category
450:See also
437:catalyst
85:613-31-0
485:Bibcode
421:ethanol
332:Density
316:180.250
160:PubChem
559:: 48.
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431:using
384:is an
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51:Names
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399:as a
241:InChI
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129:11446
98:JSmol
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