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Catalog Number:
43917
CAS Number:
4295-36-7
2,3-Dihydro-4(1 H )-quinolinone
Purity:
≥ 98% (CG)
Synonym(s):
1,2,3,4-tétrahydro-4-quinolinone, 1,2,3,4-tétrahydro-4-quinolone, 2,3-Dihydroquinolin-4(1 H )-one
Documents
$201.40 /1G
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Product Information

2,3-Dihydro-4(1H)-quinolinone is a versatile compound with significant relevance in pharmaceuticals and organic synthesis. This heterocyclic compound, also known as 4-quinolinone, exhibits unique properties that make it a valuable intermediate in the synthesis of various bioactive molecules. Its structure allows for diverse modifications, enabling researchers to explore its potential in drug development, particularly in the creation of anti-inflammatory and antimicrobial agents.

In addition to its pharmaceutical applications, 2,3-Dihydro-4(1H)-quinolinone is utilized in the development of dyes and pigments, showcasing its versatility across different industries. Its ability to act as a building block in complex organic reactions highlights its importance in synthetic chemistry. Researchers and industry professionals can leverage this compound to enhance their projects, benefiting from its unique reactivity and potential for innovation in various applications.

Synonyms
1,2,3,4-tétrahydro-4-quinolinone, 1,2,3,4-tétrahydro-4-quinolone, 2,3-Dihydroquinolin-4(1 H )-one
CAS Number
4295-36-7
Purity
≥ 98% (CG)
Molecular Formula
C 9 H 9 NON
Molecular Weight
147.18
MDL Number
MFCD00666394
PubChem ID
117158
Melting Point
42 - 46 °C
Appearance
Poudre cristalline blanche à jaune à orange
Boiling Point
167 °C/8 mmHg
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
1,2,3,4-tétrahydro-4-quinolinone, 1,2,3,4-tétrahydro-4-quinolone, 2,3-Dihydroquinolin-4(1 H )-one
CAS Number
4295-36-7
Purity
≥ 98% (CG)
Molecular Formula
C 9 H 9 NON
Molecular Weight
147.18
MDL Number
MFCD00666394
PubChem ID
117158
Melting Point
42 - 46 °C
Appearance
Poudre cristalline blanche à jaune à orange
Boiling Point
167 °C/8 mmHg
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3-Dihydro-4(1H)-quinolinone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific receptors in the brain.
  • Antioxidant Applications: It has shown promising antioxidant properties, making it valuable in the formulation of dietary supplements and skincare products aimed at reducing oxidative stress and promoting skin health.
  • Material Science: Researchers use it in the development of advanced materials, including polymers and coatings, where its unique chemical structure contributes to enhanced durability and performance.
  • Biological Research: The compound is employed in studies investigating enzyme inhibition and cellular signaling pathways, providing insights into disease mechanisms and potential therapeutic targets.
  • Organic Synthesis: It acts as a versatile building block in organic chemistry, facilitating the creation of complex molecules with applications in various fields, including agrochemicals and fine chemicals.

Citations