• 1. The synthesis of a dinuclear anionic carbonyl derivative of manganese, [N(PPh3)2][Mn2(μ-PPh2)(CO)8], and its reactions with complexes of Group 1B and Group 8A metals to give mixed-metal clusters: comparative study of the X-ray crystal structures of [N(PPh3)2][Mn2(μ-PPh2)(CO)8], [Mn2{μ-Au(PMe2Ph)}(μ-PPh2)(CO)8], and [Mn2(μ-H)(μ-PPh2)(CO)8]
  Jonathan A. Iggo,Martin J. Mays,Paul R. Raithby,Kim Henrick J. Chem. Soc. Dalton Trans. 1984 633
• 2. Quadridentate versus quinquedentate co-ordination of some N5 and N3O2 macrocyclic ligands and an unusual thermally controlled quintet ? singlet spin transition in an iron(II) complex
  S. Martin Nelson,Paul D. A. McIlroy,Clarke S. Stevenson,Edgar K?nig,Gerhard Ritter,Joachim Waigel J. Chem. Soc. Dalton Trans. 1986 991

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Quinolines and derivatives Aminoquinolines and derivatives

6-Aminoquinoline: A Comprehensive Overview

6-Aminoquinoline, also known by its CAS number CAS No. 580-15-4, is a heterocyclic organic compound that has garnered significant attention in various scientific and industrial fields. This compound, with the molecular formula C9H7N3, belongs to the quinoline family and is characterized by its unique chemical structure and versatile applications.

The structure of 6-Aminoquinoline consists of a quinoline ring with an amino group (-NH2) attached at the sixth position. This positioning imparts distinct chemical properties, making it a valuable intermediate in organic synthesis. The compound is widely used in the pharmaceutical industry, particularly in the development of antimalarial drugs, due to its ability to interact with specific biological targets.

Recent advancements in synthetic chemistry have led to innovative methods for the production of 6-Aminoquinoline. Researchers have explored various catalysts and reaction conditions to optimize its synthesis, ensuring higher yields and improved purity. These developments have not only enhanced the efficiency of production but also opened new avenues for its application in advanced materials science.

In the field of materials science, 6-Aminoquinoline has been utilized as a precursor for the synthesis of conductive polymers and metal-organic frameworks (MOFs). Its ability to coordinate with metal ions makes it an ideal candidate for constructing porous materials with applications in gas storage and catalysis. Furthermore, studies have shown that 6-Aminoquinoline-based MOFs exhibit exceptional stability under harsh conditions, making them suitable for industrial applications.

The biological activity of 6-Aminoquinoline has also been a focal point of recent research. Scientists have investigated its potential as an antimicrobial agent, particularly against drug-resistant bacterial strains. Experimental results indicate that 6-Aminoquinoline derivatives can inhibit bacterial growth by disrupting cellular membranes, offering a promising solution to the global challenge of antibiotic resistance.

In addition to its pharmacological applications, 6-Aminoquinoline has found utility in analytical chemistry as a fluorescent probe for detecting metal ions in aqueous solutions. Its fluorescence properties are highly sensitive to environmental changes, enabling precise detection of contaminants such as heavy metals in water samples.

The demand for CAS No. 580-15-4-based compounds continues to grow across multiple industries due to their versatility and adaptability. As researchers delve deeper into understanding the compound's properties, new applications are expected to emerge, further solidifying its role in modern science and technology.

• 23043-63-2(2,7-Acridinediamine)
• 581-29-3(3-Acridinamine)
• 581-28-2(2-Aminoacridine)
• 3407-94-1(2,6-Acridinediamine)
• 611-34-7(quinolin-5-amine)
• 23043-62-1(2,9-Acridinediamine)
• 134901-21-6(Platinum,dichlorobis(6-quinolinamine-N1)-, (SP-4-2)- (9CI))
• 578-68-7(quinolin-4-amine)
• 580-19-8(7-Aminoquinoline)
• 146614-41-7(5-Aminoquinoline)