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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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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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538:Bass, K. C. (1962). "9,10-Dihydroanthracene".
502:Ullmann's Encyclopedia of Industrial Chemistry
447: — analogue with three phenyl rings
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345:312 °C (594 °F; 585 K)
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241:Key: WPDAVTSOEQEGMS-UHFFFAOYSA-N
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379:polycyclic aromatic hydrocarbon
355:(at 25 °C , 100 kPa).
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486:10.1107/S010827018709512X
414:Bouveault–Blanc reduction
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433:bond dissociation energy
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17:9,10-Dihydroanthracene
371:9,10-Dihydroanthracene
262:c1ccc2c(c1)Cc3ccccc3C2
50:9,10-Dihydroanthracene
325:1.19 g mL
46:Preferred IUPAC name
478:1987AcCrC..43..537R
307: g·mol
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422:aluminium chloride
359:Infobox references
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541:Organic Syntheses
367:Chemical compound
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194:CompTox Dashboard
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400:Because the
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315:White solid
57:Identifiers
573:Anthracenes
402:aromaticity
396:Preparation
312:Appearance
271:Properties
136:100.009.398
452:References
445:Triptycene
382:anthracene
300:Molar mass
182:Z142C238GB
109:ChemSpider
85:3D model (
64:CAS Number
507:Wiley-VCH
567:Category
439:See also
426:catalyst
74:613-31-0
474:Bibcode
410:ethanol
321:Density
305:180.250
149:PubChem
548:: 48.
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420:using
373:is an
255:SMILES
40:Names
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388:as a
230:InChI
162:11940
118:11446
87:JSmol
519:ISBN
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