42835-96-1

Basic information

• Product Name: 6-Methoxy-2-Methyl-1,2,3,4-tetrahydro-quinoline
• Synonyms: 6-Methoxy-2-Methyl-1,2,3,4-tetrahydro-quinoline
• CAS NO: 42835-96-1
• Molecular Weight: 177.246
• Mol File: 42835-96-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-Methoxy-2-Methyl-1,2,3,4-tetrahydro-quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methoxy-2-Methyl-1,2,3,4-tetrahydro-quinoline(42835-96-1)
• EPA Substance Registry System: 6-Methoxy-2-Methyl-1,2,3,4-tetrahydro-quinoline(42835-96-1)

Safety Data

• Hazardous Substances Data: 42835-96-1(Hazardous Substances Data)

Upstream product

• 646039-18-1 6-methoxy-2-methyl-3,4-dihydroquinoline 
• 877-42-9 6-Bromo-2-methyl-quinoline 

Downstream Products

• 199186-62-4 (R)-6-methoxy-2-methyl-1,2,3,4-tetrahydroquinoline 
• 199186-62-4 (S)-6-methoxy-2-methyl-1,2,3,4-tetrahydroquinoline 
• 1078-28-0 6-methoxyquinaldine 
• 99540-15-5 4-(3'-methoxyphenyl)-N,N-dimethyl-2-butanamine 

Relevant articles and documents

Synthesis of Quinolines and 2H-Dihydropyrroles by Nucleophilic Substitution at the Nitrogen Atom of Oxime Derivatives

Isomerization of oxime derivatives was researched in detail to find out the methods for the syn-anti isomerization of O-substituted oximes. Based on these findings were developed simple methods for the preparation of aza-heterocycles from both stereoisomers of oximes. Quinolines were synthesized from β-aryl ketone oximes by treatment with trifluoroacetic anhydride and 4-chloranil. γ,δ-Unsaturated O-methoxyacetyloximes were transformed to 2H-dihydropyrroles by reaction with methoxy-acetic acid.