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CS-W001157 4
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4-Bromo-9-phenyl-9H-carbazole

  • CAS No. 1097884-37-1

  • Cat. No. CS-0102869
  • Purity≥97%
  • MDL No.MFCD29067336

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

4-Bromo-9-phenyl-9H-carbazole|CS-0102869

Structure of 1097884-37-1

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General Information

  • CAS No. 1097884-37-1
  • Cat. No. CS-0102869
  • Purity ≥97%
  • MDL No. MFCD29067336
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₁₂BrN
  • Molecular Weight 322.20
  • Synonym(s) 4-Bromo-N-phenylcarbazole
  • SMILES BrC1=CC=CC(N2C3=CC=CC=C3)=C1C4=C2C=CC=C4

Description

4-Bromo-9-phenyl-9H-carbazole is a brominated carbazole derivative featuring a phenyl group at the 9-position, enhancing its conjugation and electronic properties. This bench-stable compound integrates readily into cross-coupling reactions, serving as a robust building block for functionalized materials in organic electronics and photovoltaics.

Application

4-Bromo-9-phenyl-9H-carbazole serves as a versatile building block in the synthesis of functionalized carbazole scaffolds, enabling palladium-catalyzed cross-coupling reactions for C–C bond formation. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the phenyl group enhances π-conjugation and electronic stability. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for applications in organic electronics and medicinal chemistry research.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

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Computational Chemistry Data

  • TPSA   4.93
  • LogP   5.5462
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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