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Catalog Number:
17123
CAS Number:
129722-34-5
7-(4-Bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one
Purity:
≥ 98.5% (assay)
Synonym(s):
3,4-Dihydro-7-(4-bromobutoxy)-2(1H-quinolinone
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Product Information

7-(4-Bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one is a versatile compound recognized for its unique chemical structure and potential applications in various fields. This compound features a bromobutoxy group that enhances its reactivity and solubility, making it an excellent candidate for research and development in medicinal chemistry. Its quinoline core is known for its biological activity, which can be leveraged in the synthesis of novel pharmaceuticals, particularly in the development of anti-cancer and anti-inflammatory agents. Researchers have explored its potential in drug design, where its ability to interact with biological targets can lead to the discovery of new therapeutic compounds.

In addition to its pharmaceutical applications, this compound can also be utilized in the development of agrochemicals and materials science, where its properties may contribute to the formulation of effective pesticides or advanced materials. The unique combination of its structural features and functional groups allows for a wide range of modifications, making it a valuable building block in organic synthesis. As industries continue to seek innovative solutions, 7-(4-Bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one stands out as a promising compound for future research and application.

Synonyms
3,4-Dihydro-7-(4-bromobutoxy)-2(1H-quinolinone
CAS Number
129722-34-5
Purity
≥ 98.5% (assay)
Molecular Formula
C13H16BrNO2
Molecular Weight
298.18
MDL Number
MFCD06658540
PubChem ID
10542064
Melting Point
107-114º C
Appearance
White to light yellow crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
3,4-Dihydro-7-(4-bromobutoxy)-2(1H-quinolinone
CAS Number
129722-34-5
Purity
≥ 98.5% (assay)
Molecular Formula
C13H16BrNO2
Molecular Weight
298.18
MDL Number
MFCD06658540
PubChem ID
10542064
Melting Point
107-114º C
Appearance
White to light yellow crystalline powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

7-(4-Bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is explored for its potential therapeutic effects, particularly in creating new medications targeting neurological disorders.
  • Biological Research: It serves as a valuable tool in studying cellular processes and signaling pathways, aiding researchers in understanding disease mechanisms.
  • Material Science: The compound's unique properties make it suitable for developing advanced materials, including coatings and polymers with enhanced performance characteristics.
  • Drug Delivery Systems: Its chemical structure can be modified to improve the efficacy of drug delivery systems, ensuring targeted release and better patient outcomes.
  • Environmental Studies: Researchers utilize it to investigate the effects of chemical compounds on ecosystems, contributing to the development of safer chemicals.

Citations