7498-45-5

Basic information

• Product Name: (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone
• CAS NO: 7498-45-5
• Molecular Formula: C₁₆H₁₆N₂O₂
• Molecular Weight: 268.3104
• Mol File: 7498-45-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 475.6°C at 760 mmHg
• Flash Point: 241.4°C
• Density: 1.21g/cm³
• Vapor Pressure: 3.27E-09mmHg at 25°C
• Refractive Index: 1.605
• CAS DataBase Reference: (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone(7498-45-5)
• EPA Substance Registry System: (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone(7498-45-5)

Safety Data

• Hazardous Substances Data: 7498-45-5(Hazardous Substances Data)

Usage

Description

(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone is a complex organic molecule belonging to the class of quinoline derivatives. It features a heterocyclic quinoline ring and a pyridine ring, with the molecular formula C17H16N2O2. (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone is known for its potential medicinal properties and is a subject of interest for further investigation and potential drug development.

Uses

Used in Pharmaceutical Research:
(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone is used as a research compound for its potential medicinal properties. The unique chemical structure of this compound makes it a valuable candidate for exploring new therapeutic applications in the pharmaceutical industry.
Used in Drug Development:
In the field of drug development, (6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone serves as a starting point for the design and synthesis of new drugs. Its specific chemical structure and properties allow researchers to modify and optimize it for targeted therapeutic effects.
Used in Chemical Synthesis:
(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone is also utilized as a key intermediate in the synthesis of other complex organic molecules. Its presence in various chemical reactions can lead to the creation of novel compounds with diverse applications across different industries.
Used in Academic Research:
(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)(pyridin-3-yl)methanone is employed as a subject of study in academic research, particularly in the fields of organic chemistry, medicinal chemistry, and pharmacology. Researchers use it to gain insights into the structure-activity relationships of quinoline derivatives and to develop a deeper understanding of their potential applications in medicine.