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CS-W001157 4
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1,3,6,8-Tetramethyl-9H-carbazole

  • CAS No. 6558-85-6

  • Cat. No. CS-0378298
  • Purity≥98%
  • MDL No.MFCD18450169

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

1,3,6,8-Tetramethyl-9H-carbazole|CS-0378298

Structure of 6558-85-6

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General Information

  • CAS No. 6558-85-6
  • Cat. No. CS-0378298
  • Purity ≥98%
  • MDL No. MFCD18450169
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₁₇N
  • Molecular Weight 223.31
  • Synonym(s) 9H-Carbazole,1,3,6,8-tetramethy
  • SMILES CC1=CC(C)=CC2=C1NC3=C2C=C(C)C=C3C

Description

1,3,6,8-Tetramethyl-9H-carbazole features a sterically shielded carbazole core with methyl groups at key positions, enhancing stability and solubility. This electron-rich scaffold serves as a robust building block in organic semiconductors and fluorescent materials, enabling efficient charge transport and emission in optoelectronic applications.

Application

1,3,6,8-Tetramethyl-9H-carbazole serves as a robust, bench-stable building block for the synthesis of functionalized carbazole scaffolds. Its methyl substituents enhance solubility and reduce aggregation, facilitating purification and handling. The compound functions effectively in electrophilic substitution and transition-metal-catalyzed coupling reactions, enabling access to advanced materials and heterocyclic intermediates with high regiocontrol and yield.

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

Quality Control

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Computational Chemistry Data

  • TPSA   15.79
  • LogP   4.55478
  • H_Acceptors   0
  • H_Donors   1
  • Rotatable_Bonds   0

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