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Difenilmetan
	1,1'-methanediyldibenzene
Drugi nazivi	benzylbenzene
Identifikacija
CAS registarski broj	101-81-5
PubChem	7580
ChemSpider	7299
MeSH	Diphenylmethane
Jmol-3D slike	Slika 1
SMILES
	c1c(cccc1)Cc2ccccc2
InChI
	InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2 ; Kod: CZZYITDELCSZES-UHFFFAOYSA-N InChI=1/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2; Kod: CZZYITDELCSZES-UHFFFAOYAV
Svojstva
Molekulska formula	C13H12
Molarna masa	168.234
Agregatno stanje	bezbojno ulje
Gustina	1.006 g/mL
Tačka topljenja	22-24 °C
Tačka ključanja	264 °C
Rastvorljivost u vodi	nepolarni organski rastvarač
Opasnost
Opasnost u toku rada	zapaljiv
Tačka paljenja	>230 °F
Srodna jedinjenja
Srodna jedinjenja	Difenilmetanol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Difenilmetan je organsko jedinjenje sa formulom (C₆H₅)₂CH₂.^[4]^[5] Ovo jedinjenje se sastoji od metana kod koga su dva atoma vodonika zamenjena fenil grupama. Difenilmetan je često korišteni skeleton u organskoj hemiji. Difenilmetilna grupa je poznata kao benzhidril.

On se priprema reakcijom benzil hlorida sa benzenom u prisustvu Luisove kiseline kao što je aluminijum trihlorid:^[6]

C₆H₅CH₂Cl + C₆H₆ → (C₆H₅)₂CH₂ + HCl

Povezano

Benzhidrilna jedinjenja

Reference

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
↑ McMurry John E. (1992). Fundamentals of Organic Chemistry (3rd izd.). Belmont: Wadsworth. ISBN 0-534-16218-5.
↑ W. W. Hartman and Ross Phillips (1943), „Diphenylmethane”, Organic Syntheses ; Coll. Vol. 2: 232

Literatura

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[Clayden1st-4] Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.

[McMurry3rd-5] McMurry John E. (1992). Fundamentals of Organic Chemistry (3rd izd.). Belmont: Wadsworth. ISBN 0-534-16218-5.

[6] W. W. Hartman and Ross Phillips (1943), „Diphenylmethane”, Organic Syntheses ; Coll. Vol. 2: 232

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