2-Chloro-9,10-diphenylanthracene

2-chloro-9,10-diphenyl-anthracene
2-Chloro-9,10-diphenylanthracene molecule
Names
Preferred IUPAC name
2-Chloro-9,10-diphenylanthracene
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C26H17Cl/c27-20-15-16-23-24(17-20)26(19-11-5-2-6-12-19)22-14-8-7-13-21(22)25(23)18-9-3-1-4-10-18/h1-17H checkY
    Key: PLMFIWDPKYXMGE-UHFFFAOYSA-N checkY
  • InChI=1/C26H17Cl/c27-20-15-16-23-24(17-20)26(19-11-5-2-6-12-19)22-14-8-7-13-21(22)25(23)18-9-3-1-4-10-18/h1-17H
    Key: PLMFIWDPKYXMGE-UHFFFAOYAZ
  • Clc4ccc3c(c1ccccc1c(c2ccccc2)c3c4)c5ccccc5
Properties
C26H17Cl
Molar mass 364.87 g·mol−1
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

2-Chloro-9,10-diphenylanthracene is a fluorescent dye used in glow sticks for a blue-green glow.[1] It is a chlorinated derivative of 9,10-diphenylanthracene.[2]

See also

References

  1. ^ Jaworski, Jan S.; Leszczyński, Piotr; Filipek, Sławomir (1997-12-20). "Rates of the halide ion cleavage from halo-9,10-diphenylanthracene anion radicals in DMF". Journal of Electroanalytical Chemistry. 440 (1): 163–167. doi:10.1016/S0022-0728(97)80052-6. ISSN 1572-6657.
  2. ^ Evans, John F.; Blount, Henry N. (February 1976). "Reactions of cation radicals of EE [electron capture] systems. III. Chlorination of 9,10-diphenylanthracene". The Journal of Organic Chemistry. 41 (3): 516–519. doi:10.1021/jo00865a022. ISSN 0022-3263.
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