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CS-W001157 4
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6-Bromo-7-fluoro-1,2,3,4-tetrahydroquinoline

  • CAS No. 1235440-09-1

  • Cat. No. CS-0443186
  • Purity≥98%
  • MDL No.None

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

6-Bromo-7-fluoro-1,2,3,4-tetrahydroquinoline|CS-0443186

Structure of 1235440-09-1

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General Information

  • CAS No. 1235440-09-1
  • Cat. No. CS-0443186
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₉BrFN
  • Molecular Weight 230.08
  • Synonym(s) None
  • SMILES C1CC2=CC(=C(C=C2NC1)F)Br

Description

6-Bromo-7-fluoro-1,2,3,4-tetrahydroquinoline features a sterically accessible tetrahydroquinoline core with strategically positioned bromo and fluoro substituents. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions and serves as a key building block for bioactive heterocycles in medicinal chemistry.

Application

6-Bromo-7-fluoro-1,2,3,4-tetrahydroquinoline serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds in API development.

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-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   12.03
  • LogP   2.9463
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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