CAS 612-60-2
:7-Methylchinolin
- Ai3-00850
- Brn 0110317
- Ccris 2895
- Nsc 65665
- Quinoline, 7-methyl-
- m-Toluquinoline
- 5-20-07-00402 (Beilstein Handbook Reference)
- 7-Methylquinoline
- 7-METHYLQUINOLINE, (CONTAINS-20% 5-FORM) 75+%
- 7-Methylquinoline,97%
- Quinolinol,7-methyl-
- 7-METHYLQUINOLINE: TECH., 70%
- 7-methyquinoline
- 7-Methylquinoline (contains-25% 5-form)
- 7-Methylquinoline, tech. 70%, remainder mainly 5-isomer
- 7-methyl-quinolin
- 7-Methylquinolinol
- 7-Methylquinoline,tech.70%
- 7-Methylquiuoline
- Weitere Synonyme anzeigen
7-Methylquinoline (contains 25% 5-form at maximum)
CAS:Formel:C10H9NReinheit:>75.0%(GC)Farbe und Form:Colorless to Light orange to Yellow clear liquidMolekulargewicht:143.197-Methylquinoline
CAS:Formel:C10H9NReinheit:>98.0%(GC)Farbe und Form:White or Colorless to Almost white or Almost colorless powder to lump to clear liquidMolekulargewicht:143.197-Methylquinoline, 97%
CAS:7-methylquinolineFormel:C10H9NReinheit:97%Farbe und Form:Pale yellow, Low melting solid / liquidMolekulargewicht:143.197-Methylquinoline
CAS:7-MethylquinolineFormel:C10H9NReinheit:97%Farbe und Form: brown low melting solidMolekulargewicht:143.19g/molm-Toluquinoline
CAS:Kontrolliertes ProduktApplications m-Toluquinoline is a reagent used in the preparation of diarylmethylpiperazines as potent opioid receptor agonists with improved side effects. Also used in the preparation of novel pyrazine compounds derived from 2-phenylquinolin-7-yl which act as potent insulin-like growth factor-I receptor inhibitors.
References Plobeck, N. et al.: J. Med. Chem., 43, 3878 (2000); Mulvihill, M. et al.: Bioorg Med. Chem. Lett., 16, 1359 (2008);Formel:C10H9NFarbe und Form:Off-WhiteMolekulargewicht:143.1857-Methylquinoline
CAS:7-Methylquinoline is an organic compound that can be used to synthesize antimalarial drugs. It is a quinoline derivative with a methyl group at the 7th position. The structure of 7-methylquinoline contains a nitrogen atom and hydrogen atoms, which are bonded to fluorine, chlorine, and bromine atoms. This molecule has been shown to be stable in the presence of Friedel-Crafts catalysts and chloride ions. The reaction mechanism for 7-methylquinoline is intramolecular hydrogen transfer from the chloroform molecule to the quinoline ring system. The formation rate for this compound is slow because it requires two steps: nucleophilic substitution and electrophilic addition reactions.
Formel:C10H9NReinheit:Min. 95%Molekulargewicht:143.19 g/mol






