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Diphenyldichloromethane information


Diphenyldichloromethane
Names
Preferred IUPAC name
1,1′-(Dichloromethylene)dibenzene
Other names
Dichlorodiphenylmethane
Identifiers
CAS Number
  • 2051-90-3 checkY
3D model (JSmol)
  • Interactive image
Beilstein Reference
1910601
ChemSpider
  • 15492 checkY
ECHA InfoCard 100.016.486 Edit this at Wikidata
PubChem CID
  • 16327
UNII
  • 81FEZ29AK6 checkY
CompTox Dashboard (EPA)
  • DTXSID9062148 Edit this at Wikidata
InChI
  • InChI=1S/C13H10Cl2/c14-13(15,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H checkY
    Key: OPTDDWCXQQYKGU-UHFFFAOYSA-N checkY
SMILES
  • c1ccc(cc1)C(c2ccccc2)(Cl)Cl
Properties
Chemical formula
C13H10Cl2
Molar mass 237.12 g·mol−1
Appearance colorless solid
Density 1.235 g/cm3
Melting point 146 to 150 °C (295 to 302 °F; 419 to 423 K)[2]
Boiling point 193 °C (379 °F; 466 K) at 32 torr[1]
Hazards
Flash point 110 °C (230 °F; 383 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Diphenyldichloromethane is an organic compound with the formula (C6H5)2CCl2. It is a colorless solid that is used as a precursor to other organic compounds.

  1. ^ Andrews, L. J.; W. W. Kaeding (1951). "The Formation of Benzophenone and its Diethylketal in the Ethanolysis of Diphenyldichloromethane". Journal of the American Chemical Society. 73 (3): 1007–1011. doi:10.1021/ja01147a036. ISSN 0002-7863.
  2. ^ Ballester, Manuel; Juan Riera-Figueras; Juan Castaner; Carlos Badfa; Jose M. Monso (1971). "Inert carbon free radicals. I. Perchlorodiphenylmethyl and perchlorotriphenylmethyl radical series". Journal of the American Chemical Society. 93 (9): 2215–2225. doi:10.1021/ja00738a021. ISSN 0002-7863.

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Diphenyldichloromethane

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Diphenyldichloromethane is an organic compound with the formula (C6H5)2CCl2. It is a colorless solid that is used as a precursor to other organic compounds...

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Phosphorus pentachloride

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example, benzophenone and phosphorus pentachloride react to give the diphenyldichloromethane: (C6H5)2CO + PCl5 → (C6H5)2CCl2 + POCl3 The electrophilic character...

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Benzophenone

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with carbon tetrachloride followed by hydrolysis of the resulting diphenyldichloromethane. It can also be prepared by Friedel–Crafts acylation of benzene...

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Tetraphenylethylene

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supramolecular chemistry. Tetraphenylethene can be synthesized from diphenyldichloromethane. Banerjee, Moloy; Susanna J. Emond; Sergey V. Lindeman; Rajendra...

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Thiobenzophenone

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thiobenzophenone involves the reaction of sodium hydrosulfide and diphenyldichloromethane: Ph2CCl2 + 2 NaSH → Ph2C=S + 2 NaCl + H2S An updated method involves...

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