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Ethyl 2-(3-bromoquinolin-6-yl)acetate

  • CAS No. 1393353-34-8

  • Cat. No. CS-D0355
  • Purity≥96%
  • MDL No.MFCD17215806

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

Ethyl 2-(3-bromoquinolin-6-yl)acetate|CS-D0355

Structure of 1393353-34-8

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General Information

  • CAS No. 1393353-34-8
  • Cat. No. CS-D0355
  • Purity ≥96%
  • MDL No. MFCD17215806
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₁₂BrNO₂
  • Molecular Weight 294.14
  • Synonym(s) 6-Quinolineacetic acid, 3-bromo-, ethyl ester
  • SMILES O=C(OCC)CC1=CC=C2N=CC(Br)=CC2=C1

Description

Ethyl 2-(3-bromoquinolin-6-yl)acetate features a brominated quinoline scaffold paired with an acrylate ester, enabling direct incorporation into cross-coupling and cyclization cascades. This bench-stable, moisture-tolerant building block delivers efficient access to functionalized heterocycles in medicinal chemistry and materials synthesis.

Application

Ethyl 2-(3-bromoquinolin-6-yl)acetate serves as a versatile building block for constructing quinoline-based scaffolds in medicinal chemistry and materials science. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the ester group offers compatibility with reduction, hydrolysis, and further functionalization. Its bench-stable nature and predictable reactivity facilitate efficient synthesis of complex heterocycles and API intermediates.

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   39.19
  • LogP   3.1029
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   3

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