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9,10-Dibromoanthracene

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CAS:523-27-3
Purity:99.5%+ Package:10kg;USD|100kg;USD|1000kg;USD
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CAS:523-27-3
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Products Intro: Product Name:9,10-Dibromoanthracene
CAS:523-27-3
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9,10-Dibromoanthracene manufacturers

  • 9,10-Dibromoanthracene
  • 9,10-Dibromoanthracene pictures
  • $0.00 / 1KG
  • 2024-11-19
  • CAS:523-27-3
  • Min. Order: 1KG
  • Purity: 98%min
  • Supply Ability: 30tons/month
  • 9,10-Dibromoanthracene
  • 9,10-Dibromoanthracene pictures
  • $450.00 / 1KG
  • 2024-11-19
  • CAS:523-27-3
  • Min. Order: 1KG
  • Purity: 98%+
  • Supply Ability: 300MT/year
  • 9,10-Dibromoanthracene
  • 9,10-Dibromoanthracene pictures
  • $100.00 / 1KG
  • 2023-12-24
  • CAS:523-27-3
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
9,10-Dibromoanthracene Basic information
Product Name:9,10-Dibromoanthracene
Synonyms:9,I O-Dibromanthracen;9,10-DIBROMO ANTHRACENEN;9,10-Dibromoanthracene,96%;Anthracene,9,10-dibromo-;ms-Dibromoanthracene;9,10-DIBROMOANTHRACENE;9,10-DIRBOMOANTHRACENE;9,1O-dibromoanthracene
CAS:523-27-3
MF:C14H8Br2
MW:336.02
EINECS:208-342-4
Product Categories:Miscellaneous;Aromatic Compounds;Electronic Chemicals;Anthracenes;Anthracene series;Aryl;C13 to C37+;Halogenated Hydrocarbons;OLED materrials;C13 to C37+;Building Blocks;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks;OLED
Mol File:523-27-3.mol
9,10-Dibromoanthracene Structure
9,10-Dibromoanthracene Chemical Properties
Melting point 223-224 °C (lit.)
Boiling point 342.21°C (rough estimate)
density 1.7167 (estimate)
refractive index 1.6300 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform
form Fluffy Powder
color Yellow to yellow-green
Water Solubility Soluble in water.
Merck 14,3018
BRN 1912109
InChIKeyBRUOAURMAFDGLP-UHFFFAOYSA-N
CAS DataBase Reference523-27-3(CAS DataBase Reference)
NIST Chemistry ReferenceAnthracene, 9,10-dibromo-(523-27-3)
EPA Substance Registry SystemAnthracene, 9,10-dibromo- (523-27-3)
Safety Information
Hazard Codes Xi,N
Risk Statements 36/37/38-50/53
Safety Statements 37/39-26-61-60-36
RIDADR UN 3077
WGK Germany 3
TSCA Yes
HS Code 29039990
MSDS Information
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9,10-Dibromoanthracene English
ACROS English
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9,10-Dibromoanthracene Usage And Synthesis
Description9,10-Dibromoanthracene is an organic chemical compound containing anthracene with two bromine atoms substituted on its central ring. As a symmetrically brominated anthracene derivative, it is bearing functional groups to extend its conjugation further mainly via C-C bond forming i.e. Stille and Suzuki coupling reactions. It is notable in that it was the first single molecule to have a chemical reaction observed by an atomic force microscope and scanning tunneling microscopy. It is a low-molecular-weight organic semiconductor. It can used as an initiator in visible-spectrum solar-light-mediated benzylic C–H oxygenation through solar light or the blue LED activate[1-2].
Chemical PropertiesYellow to yellow-green fluffy powder. Melting point 226°C. It can be sublimated and oxidized to generate anthraquinone. It is soluble in hot benzene and hot toluene, but only slightly soluble in alcohol, ether, and cold benzene. It is insoluble in water.
Uses9,10-Dibromoanthracene is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.
Preparation9,10-Dibromoanthracene is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.
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Origin9,10-Dibromoanthracene was first synthesized in 1923 by Ian (formerly Isidor) M. Heilbron and John S. Heaton, chemists working at the University of Liverpool.
Purification MethodsRecrystallise it from toluene, xylene or CCl4 (yellow needles), and sublime it in a vacuum [Johnston et al. J Am Chem Soc 109 1291 1987]. [Heilbron & Heaton Org Synth Coll Vol I 207 1941, Beilstein 5 H 665.]
References[1] Santra S, et al. Visible-Spectrum Solar-Light-Mediated Benzylic C–H Oxygenation Using 9,10-Dibromoanthracene As an Initiator. The Journal of Organic Chemistry, 2020; 86: 1164–1171.
[2] Watanabe M. Formation of aligned needle-like crystals of 9,10-dibromoanthracene in small droplets. Journal of Applied Polymer Science, 2023; 140: e54515.
Tag:9,10-Dibromoanthracene(523-27-3) Related Product Information
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