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CS-W001157 4
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2,3,6,7,14,15-Hexabromo-9,10-dihydro-9,10-[1,2]benzenoanthracene

  • CAS No. 55805-81-7

  • Cat. No. CS-0111314
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

2,3,6,7,14,15-Hexabromo-9,10-dihydro-9,10-[1,2]benzenoanthracene|CS-0111314

Structure of 55805-81-7

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General Information

  • CAS No. 55805-81-7
  • Cat. No. CS-0111314
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₈Br₆
  • Molecular Weight 727.70
  • Synonym(s) 9,10[1,2]-Benzenoanthracene, 2,3,6,7,14,15-hexabromo-9,10-dihydro-
  • SMILES BrC1=CC2=C(C=C1Br)C3C4=C(C=C(Br)C(Br)=C4)C2C5=C3C=C(Br)C(Br)=C5

Description

This hexabrominated dihydrobenzenoanthracene features six bromine substituents strategically positioned to enhance electron deficiency and facilitate cross-coupling reactions. The rigid, planar core supports π-stacking interactions, while the brominated framework enables precise functionalization in materials synthesis. Bench-stable and moisture-tolerant, it serves as a robust building block for advanced organic semiconductors and molecular architectures.

Application

2,3,6,7,14,15-Hexabromo-9,10-dihydro-9,10-[1,2]benzenoanthracene serves as a highly functionalized polycyclic building block for the synthesis of brominated aromatic scaffolds. Its six bromine substituents enable versatile cross-coupling reactions, including Suzuki and Stille couplings, facilitating access to complex molecular architectures. The dihydroanthracene core offers enhanced bench stability and compatibility with standard reaction conditions, supporting efficient purification and scalability in synthetic workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   9.2488
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   0

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