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5-Bromo-7H-benzo[c]carbazole

  • CAS No. 131409-18-2

  • Cat. No. CS-0156026
  • Purity≥98%
  • MDL No.MFCD30063204

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

5-Bromo-7H-benzo[c]carbazole|CS-0156026

Structure of 131409-18-2

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General Information

  • CAS No. 131409-18-2
  • Cat. No. CS-0156026
  • Purity ≥98%
  • MDL No. MFCD30063204
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₁₀BrN
  • Molecular Weight 296.16
  • Synonym(s) None
  • SMILES C1=CC=C2C(=C1)C(=CC3=C2C4=CC=CC=C4N3)Br

Description

5-Bromo-7H-benzo[c]carbazole delivers a rigid, electron-deficient heteroaromatic scaffold ideal for constructing π-conjugated systems in organic electronics. The bromine substituent enables direct functionalization via cross-coupling, while the fused carbazole core provides enhanced stability and tunable optoelectronic properties under standard conditions.

Application

5-Bromo-7H-benzo[c]carbazole serves as a versatile building block for the synthesis of polycyclic aromatic systems and heterocyclic scaffolds relevant to medicinal chemistry. The bromine substituent enables facile palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and extended conjugated frameworks. Its inherent stability and compatibility with standard synthetic protocols make it a practical choice for iterative functionalization and library generation in drug discovery workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

Quality Control

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Computational Chemistry Data

  • TPSA   15.79
  • LogP   5.2368
  • H_Acceptors   0
  • H_Donors   1
  • Rotatable_Bonds   0

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