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CS-W001157 4
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1-Chloro-9H-carbazole

  • CAS No. 5599-70-2

  • Cat. No. CS-0043183
  • Purity≥97%
  • MDL No.None

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

1-Chloro-9H-carbazole|CS-0043183

Structure of 5599-70-2

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General Information

  • CAS No. 5599-70-2
  • Cat. No. CS-0043183
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₈ClN
  • Molecular Weight 201.65
  • Synonym(s) 1-chlorocarbazole
  • SMILES ClC1=CC=CC2=C1NC3=C2C=CC=C3

Description

1-Chloro-9H-carbazole serves as a versatile electrophilic building block in synthetic organic chemistry, featuring a chlorine atom poised for nucleophilic substitution at the C1 position. The carbazole core provides electron-rich aromatic character, enabling integration into conjugated systems for materials science and pharmaceutical applications. This bench-stable compound facilitates efficient coupling reactions under mild conditions.

Application

1-Chloro-9H-carbazole serves as a versatile building block in synthetic organic chemistry, enabling efficient functionalization at the C1 position via palladium-catalyzed cross-coupling reactions. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for constructing complex heterocyclic architectures, including those found in pharmaceutical intermediates and advanced materials.

Safety Information

Download SDS
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   15.79
  • LogP   3.9745
  • H_Acceptors   0
  • H_Donors   1
  • Rotatable_Bonds   0

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