7461-11-2

Basic information

• Product Name: 2-chloroquinolin-8-aMine
• Synonyms: 2-chloroquinolin-8-aMine
• CAS NO: 7461-11-2
• Molecular Formula: C9H7ClN2
• Molecular Weight: 178.61828
• Mol File: 7461-11-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 346.1 °C at 760 mmHg
• Flash Point: 163.1 °C
• Appearance: /
• Density: 1.363 g/cm³
• Vapor Pressure: 5.89E-05mmHg at 25°C
• Refractive Index: 1.712
• CAS DataBase Reference: 2-chloroquinolin-8-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloroquinolin-8-aMine(7461-11-2)
• EPA Substance Registry System: 2-chloroquinolin-8-aMine(7461-11-2)

Safety Data

• Hazardous Substances Data: 7461-11-2(Hazardous Substances Data)

Usage

General Description

2-chloroquinolin-8-amine is a chemical compound with the molecular formula C9H7ClN2. It is an amino derivative of quinoline, a heterocyclic compound commonly found in dyes, antimalarial drugs, and other pharmaceuticals. 2-chloroquinolin-8-amine has a chlorine atom attached to the 2 position of the quinoline ring and an amine group at the 8 position. Its structure and properties make it suitable for use in organic synthesis and as a building block for the preparation of various pharmaceutical compounds and other organic molecules. Additionally, its potential biological activities make it a subject of interest in medicinal chemistry research.

InChI:InChI=1/C9H7ClN2/c10-8-5-4-6-2-1-3-7(11)9(6)12-8/h1-5H,11H2

Upstream product

• 4225-86-9 2-chloro-8-nitroquinoline 
• 612-62-4 2-Chloroquinoline 

Relevant articles and documents

Effects of the Distance between Radical Sites on the Reactivities of Aromatic Biradicals

Coupling of the radical sites in isomeric benzynes is known to hinder their radical reactivity. In order to determine how far apart the radical sites must be for them not to interact, the gas-phase reactivity of several isomeric protonated (iso)quinoline-and acridine-based biradicals was examined. All the (iso)quinolinium-based biradicals were found to react slower than the related monoradicals with similar vertical electron affinities (i.e., similar polar effects). In sharp contrast, the acridinium-based biradicals, most with the radical sites farther apart than in the (iso)quinolinium-based systems, showed greater reactivities than the relevant monoradicals with similar vertical electron affinities. The greater distances between the two radical sites in these biradicals lead to very little or no spin-spin coupling, and no suppression of radical reactivity was observed. Therefore, the radical sites can still interact if they are located on adjacent benzene rings and only after being separated further than that does no coupling occur. The most reactive radical site of each biradical was experimentally determined to be the one predicted to be more reactive based on the monoradical reactivity data. Therefore, the calculated vertical electron affinities of relevant monoradicals can be used to predict which radical site is most reactive in the biradicals.

Novel Sulfonaminoquinoline Hepcidin Antagonists

The present invention relates to novel hepcidin antagonists, pharmaceutical compositions comprising them and the use thereof as medicaments for the use in the treatment of iron metabolism disorders, such as, in particular, iron deficiency diseases and anemias, in particular anemias in connection with chronic inflammatory diseases.