1074-06-2

Usage

Uses

Used in Pharmaceutical Industry:
Quinoline, 2,3,4,4a,5,6,7,8-octahydrois used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form heterocyclic compounds, which are essential in drug development. Its presence in the molecular structure of certain drugs contributes to their therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, Quinoline, 2,3,4,4a,5,6,7,8-octahydrois utilized as a precursor in the production of agrochemicals, particularly those with insecticidal properties. Its natural occurrence in some plants and its inherent insect-killing capabilities make it a valuable component in developing pesticides and other crop protection agents.
Used in Chemical Research:
Quinoline, 2,3,4,4a,5,6,7,8-octahydroserves as a subject of study in chemical research for its unique properties and potential applications. Researchers explore its reactivity, stability, and interactions with other compounds to discover new uses and improve existing ones in various industries.

Downstream Products

• 110254-60-9 4-Dicyanomethylen-5,6-tetramethylen-2,3-diphenyl-1-azabicyclo<4.3.0>non-2-en 
• 110254-61-0 2-Cyanophenylmethylen-1,1a-diphenyl-1,2,5,6,6a,7,8,9a,9b-decahydro-1,9a-cyclopropa-4H-pyrrolo<3.2.1-ij>-chinolin 
• 154325-32-3 (4aR,8R,SR)-8-(p-tolylsulfinyl)-2,3,4,4a,5,6,7,8-octahydro-4a-quinolinol 
• 154325-32-3 (4aS,8S)-8-((R)-Toluene-4-sulfinyl)-3,4,5,6,7,8-hexahydro-2H-quinolin-4a-ol 
• 108201-30-5 2-(t-Butylthio)-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin 
• 131556-11-1 cis-8a-phenyldecahydroquinoline 
• 108201-28-1 2-Methoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin 
• 108201-29-2 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin 
• 108201-21-4 5,6-Tetramethylen-2,3-diphenyl-1-azabicyclo<4.3.0>non-2-en-4-on 
• 767-92-0 trans-decahydroquinoline 
• 90562-36-0 8-chloro-1,2,3,4-tetrahydroquinoline 
• 611-33-6 8-chloroquinoline 
• 139870-92-1 8a-phenyl-Δ^4,4a-octahydroquinoline 
• 139870-91-0 cis-4a-hydroxy-8a-phenyldecahydroquinoline 

Relevant academic research and scientific papers

Synthesis and Thermolysis of O-Alkyl-N-vinylhydroxylamine Derivatives

Oxoiminium salts 11 a-e and 13 a-e have been prepared from the ο-chloroketones 9 a-e by oximation via the cyclic oxime ethers 10 a-e and the cyclic imine oxides 12 a-e, followed by alkylation with "Meerwein salt".The deprotonation reaction of 11 a-e and 13 a-e yields, via the regioselectively prepared intermediates 14 a-e and 17 a-e, the α, β-unsaturated imines 15 a-e and the cyclic imines 18 a-e, respectively.