3,6-Dibromo-9-(4-bromophenyl)carbazole - ≥98%(HPLC) , CAS No.73087-83-9

CAS: 73087-83-9 Cat. No.: D154442 Molecular Weight: 480 EC Number: 808-076-4

GRADE & PURITY ≥98%(HPLC)

Synonyms

DS-5671 | 9H-Carbazole, 3,6-dibromo-9-(4-bromophenyl)- | DTXSID60453674 | C18H10Br3N | A866153 | 3,6-dibromo-9-(4-bromophenyl)carbazole | 3,6-Dibromo-9-(4-bromo-phenyl)-9H-carbazole | 3,6-Dibromo-9-(4-bromophenyl)-9H-carbazole | YSWG315 | D4563 | YCA08783

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

DS-5671 | 9H-Carbazole, 3, 6-dibromo-9-(4-bromophenyl)- | DTXSID60453674 | C18H10Br3N | A866153 | 3, 6-dibromo-9-(4-bromophenyl)carbazole | 3, 6-Dibromo-9-(4-bromo-phenyl)-9H-carbazole | 3, 6-Dibromo-9-(4-bromophenyl)-9H-carbazole | YSWG315 | D4563 | YCA08783

Specifications & Purity

≥98%(HPLC)

Storage

Room temperature

Shipped In

Normal

Purity

≥98%(HPLC)

Names and Identifiers

• Pubchem Sid: 488197112
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197112
• Canonical Smiles: C1=CC(=CC=C1N2C3=C(C=C(C=C3)Br)C4=C2C=CC(=C4)Br)Br
• IUPAC Name: 3,6-dibromo-9-(4-bromophenyl)carbazole
• InChIKey: NRTDFHUSNYJENJ-UHFFFAOYSA-N
• INCHI: 1S/C18H10Br3N/c19-11-1-5-14(6-2-11)22-17-7-3-12(20)9-15(17)16-10-13(21)4-8-18(16)22/h1-10H
• Isomeric SMILES: C1=CC(=CC=C1N2C3=C(C=C(C=C3)Br)C4=C2C=CC(=C4)Br)Br
• Molecular Weight: 480
• Reaxy-Rn: 4873544
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4873544&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Biphenyls and derivatives
        • Level5 Brominated biphenyls
          • Level6 Polybrominated biphenyls

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Biphenyls and derivatives
• Intermediate Tree Nodes: Brominated biphenyls
• Direct Parent: Polybrominated biphenyls
• Alternative Parents: Carbazoles Phenylpyrroles Indoles Bromobenzenes Aryl bromides Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Polybrominated biphenyl - Carbazole - 1-phenylpyrrole - Indole - Indole or derivatives - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as polybrominated biphenyls. These are organic aromatic compounds containing a biphenyl moiety, which is substituted at two or more ring positions by a bromine atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Melt Point(°C): 207-211℃
• Molecular Weight: 480.000 g/mol
• XLogP3: 7.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 478.834 Da
• Monoisotopic Mass: 476.836 Da
• Topological Polar Surface Area: 4.900 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 370.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Xin Pan, Ping Xue, Xiaobo Wang, Fu Chen, Yijun Gao, Mi Tang, Chengliang Wang, Zhengbang Wang.  (2022)  Boosting the energy density of organic cathode materials by designing planarized conjugated p-type polymer with multi-redox-active centers.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.137920]

2. Xinming Wu, Bin Huang, Qiguan Wang, Yan Wang.  (2019)  Thermally chargeable supercapacitor using a conjugated conducting polymer: Insight into the mechanism of charge-discharge cycle.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.05.075]