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CS-W001157 4
Total: USD 88.00

6-Bromo-3,3-dimethyl-1,2,3,4-tetrahydroquinoline

  • CAS No. 184041-19-8

  • Cat. No. CS-0520999
  • Purity≥98%
  • MDL No.None

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

6-Bromo-3,3-dimethyl-1,2,3,4-tetrahydroquinoline|CS-0520999

Structure of 184041-19-8

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General Information

  • CAS No. 184041-19-8
  • Cat. No. CS-0520999
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₄BrN
  • Molecular Weight 240.14
  • Synonym(s) None
  • SMILES CC1(C)CNC2=C(C=C(Br)C=C2)C1

Description

6-Bromo-3,3-dimethyl-1,2,3,4-tetrahydroquinoline features a brominated tetrahydroquinoline core with steric shielding from two methyl groups at the 3-position. This bench-stable scaffold integrates readily into transition-metal-catalyzed coupling reactions, offering a robust platform for synthesizing functionalized heterocycles in medicinal chemistry and materials science.

Application

6-Bromo-3,3-dimethyl-1,2,3,4-tetrahydroquinoline serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the tetrahydroquinoline core provides a rigid, electron-rich scaffold suitable for drug discovery. Its bench-stable nature and compatibility with standard functional group transformations facilitate efficient synthesis of complex heterocyclic architectures.

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   12.03
  • LogP   3.4433
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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