6931-19-7

Basic information

• Product Name: 5-METHOXYQUINOLINE
• Synonyms: 5-METHOXYQUINOLINE
• CAS NO: 6931-19-7
• Molecular Formula: C₁₀H₉NO
• Molecular Weight: 159.18456
• EINECS: -0
• Product Categories: Chemical Amines;Amines;Aromatics
• Mol File: 6931-19-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 280.1 °C at 760 mmHg
• Flash Point: 102.7 °C
• Appearance: Brown Oil
• Density: 1.13 g/cm³
• Vapor Pressure: 0.00656mmHg at 25°C
• Refractive Index: 1.61
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform
• PKA: 4.84±0.12(Predicted)
• CAS DataBase Reference: 5-METHOXYQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHOXYQUINOLINE(6931-19-7)
• EPA Substance Registry System: 5-METHOXYQUINOLINE(6931-19-7)

Safety Data

• Hazardous Substances Data: 6931-19-7(Hazardous Substances Data)

Usage

Chemical Properties

Brown Oil

Uses

5-Methoxyquinoline (cas# 6931-19-7) is a compound useful in organic synthesis.

InChI:InChI=1/C10H9NO/c1-12-10-6-2-5-9-8(10)4-3-7-11-9/h2-7H,1H3

Upstream product

• 536-90-3 m-Anisidine 
• 58750-87-1 N-tosyl-m-anisidine 
• 7022-24-4 N-(3-methoxyphenyl)methanesulfonamide 
• 333383-79-2 N-(3-methoxy-phenyl)-4-methyl-N-(3-oxo-propyl)-benzenesulfonamide 
• 333383-78-1 N-(3-methoxy-phenyl)-N-(3-oxo-propyl)-methanesulfonamide 
• 75-07-0 acetaldehyde 
• 82673-65-2 N-(2-formyl-3-methoxyphenyl)pivalamide 
• 56619-93-3 N-(3-methoxyphenyl)pivalamide 
• 927-63-9 3-dimethylaminoacrolein 
• 1611-78-5 1,3-bis-dimethylaminotrimethinium perchlorate 
• 578-67-6 quinolin-5-ol 
• 74-88-4 methyl iodide 
• 30389-37-8 5-methoxy-1,2,3,4-tetrahydroquinoline 
• 611-34-7 5-Aminoquinoline 

Downstream Products

• 946137-08-2 5-methoxy-1-(4-methoxybenzyl)-2-(trifluoromethyl)-1,2-dihydroquinoline 
• 497068-73-2 tert-butyl 5-hydroxy-3,4-dihydroquinoline-1(2H)-carboxylate 
• 61468-43-7 5-hydroxy-1,2,3,4-tetrahydroquinoline 
• 1423778-31-7 5-methoxy-2-(phenylethynyl)quinoline 
• 160893-07-2 2-chloro-5-methoxyquinoline 
• 160893-04-9 5-methoxy-2(1H)-quinolinone 
• 30389-37-8 5-methoxy-1,2,3,4-tetrahydroquinoline 

Relevant articles and documents

Potassium tert-Butoxide-Promoted Acceptorless Dehydrogenation of N-Heterocycles

Potassium tert-butoxide-promoted acceptorless dehydrogenation of N-heterocycles was efficiently realized for the generation of N-heteroarenes and hydrogen gas under transition-metal-free conditions. In the presence of KOtBu base, a variety of six- and five-membered N-heterocyclic compounds efficiently underwent acceptorless dehydrogenation to afford the corresponding N-heteroarenes and H2 gas in o-xylene at 140 °C. The present protocol provides a convenient route to aromatic nitrogen-containing compounds and H2 gas. (Figure presented.).

NOVEL QUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS FOR PREVENTING OR TREATING CANCER CONTAINING THE SAME

The present invention refers to an excellent cancer antiproliferative potency relative to the quinoline compounds, a pharmaceutically acceptable salt, or hydrate and, number of active ingredient containing bath method and pharmaceutical composition for the prevention or treatment of cancer disease relates to search, said present invention according to compound, a pharmaceutically acceptable salt thereof, or hydrate number and number and mutant kinase protein kinase activity number of excellent cancer billion billion number activity and thus, new anticancer number is useful as the effective component can be. (by machine translation)

Design, synthesis, in-vitro antiproliferative activity and kinase profile of new picolinamide based 2-amido and ureido quinoline derivatives

Abstract New 2-amido and ureido quinoline derivatives substituted with 2-N-methylamido-pyridin-4-yloxy group at the 5-position of quinoline (18 final compounds) have been designed and synthesized as anticancer sorafenib congeners. Among the synthesized de