4964-76-5

Basic information

• Product Name: 7-methoxyquinoline
• Synonyms: 7-methoxyquinoline
• CAS NO: 4964-76-5
• Molecular Formula: C₁₀H₉NO
• Molecular Weight: 159.18
• EINECS: -0
• Product Categories: Chemical Amines;Amines;Aromatics
• Mol File: 4964-76-5.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 280.1 °C at 760 mmHg
• Flash Point: 102.7 °C
• Appearance: /
• Density: 1.13 g/cm³
• Vapor Pressure: 0.00656mmHg at 25°C
• Refractive Index: 1.61
• Storage Temp.: Refrigerator
• Solubility: Chloroform
• CAS DataBase Reference: 7-methoxyquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methoxyquinoline(4964-76-5)
• EPA Substance Registry System: 7-methoxyquinoline(4964-76-5)

Safety Data

• Hazardous Substances Data: 4964-76-5(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Oil

Uses

7-Methoxyquinoline (cas# 4964-76-5) is a compound useful in organic synthesis.

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

Upstream product

• 4965-36-0 7-bromoquinoline 
• 536-90-3 m-Anisidine 
• 56-81-5 glycerol 
• 93626-91-6 5-p-methoxyphenyl-1-methyl-2-aza-1-oxapentadiene 
• 580-20-1 quinolin-7-ol 
• 74-88-4 methyl iodide 
• 333383-78-1 N-(3-methoxy-phenyl)-N-(3-oxo-propyl)-methanesulfonamide 
• 333383-79-2 N-(3-methoxy-phenyl)-4-methyl-N-(3-oxo-propyl)-benzenesulfonamide 
• 682350-96-5 7-methoxy-2-(methylthio)quinoline 
• 7022-24-4 N-(3-methoxyphenyl)methanesulfonamide 
• 58750-87-1 N-tosyl-m-anisidine 
• 1963-36-6 4-methoxycinnamaldehyde 
• 555-03-3 3-nitroanisole 
• 19500-61-9 7-methoxy-1,2,3,4-tetrahydroquinoline 

Downstream Products

• 852402-71-2 7-methoxyquinoline-2-carboxylic acid 
• 21979-60-2 7-methoxy-1-methyl-quinolinium; iodide 
• 580-20-1 quinolin-7-ol 
• 19500-61-9 7-methoxy-1,2,3,4-tetrahydroquinoline 
• 83010-83-7 7-methoxy-8-nitroquinoline 
• 128278-08-0 N-methylquinolin-7-amine 
• 58196-33-1 7-hydroxy-1,2,3,4-tetrahydroquinoline 
• 101877-76-3 1-benzoyl-7-methoxy-1,2,3,4-tetrahydro-quinoline 
• 83010-84-8 8-amino-7-methoxyquinoline 
• 1374233-04-1 C₂₄H₃₀FNO₄SSi 
• 1374233-05-2 C₁₈H₁₆FNO₃S 
• 1374233-06-3 C₂₀H₁₈FNO₅S 
• 1374233-07-4 C₁₉H₁₆FNO₅S 
• 1374229-61-4 C₂₀H₁₉FN₂O₄S 

Relevant articles and documents

Synthesis of 7-alkoxyquinolines, coumarins, and resorufins

Synthesis of the title compounds by treatment of the sodium salts of 7- quinolinol, 7-hydroxycoumarin, and resorufin with alkyl halides is described.

NOVEL COMPOUND, PHOTOACID GENERATOR CONTAINING THE COMPOUND, AND PHOTOSENSITIVE RESIN COMPOSITION CONTAINING THE PHOTOACID GENERATOR

PROBLEM TO BE SOLVED: To provide a nonionic photoacid generator with high acid generation quantum yield. SOLUTION: The present invention provides a compound represented by formula (2) (where, ring Ar is a benzene ring, naphthalene ring, thiophene ring or

A self-contained photoacid generator for super acid based on photochromic terarylene

A self-contained photoacid generator for super acid along with the photoinduced 6π-electrocyclization reaction of the terarylene backbone is demonstrated. The photoinitiated cationic polymerization of epoxy-monomers is achieved with an efficient photochem