4-methylquinoline

4-methylquinoline Basic information
Product Name:4-methylquinoline
Synonyms:4-METHYLQUINUOLINE;4-METHYLQUINOLINE 99+%;LEPIDINE, 99% (4-METHYLQUINOLINE);Lepidine(4-Methylquinoline)99%;Lepidine,98%;4-Methylquinoline, Lepidine;Lepidine ,99%;4-Methylquinoline,4-Methylquinoline, Lepidine
CAS:491-35-0
MF:C10H9N
MW:143.19
EINECS:207-734-2
Product Categories:Alkylquinolines;Quinolines;Quinoline series;Quinoline Derivertives
Mol File:491-35-0.mol
4-methylquinoline Structure
4-methylquinoline Chemical Properties
Melting point 9-10 °C(lit.)
Boiling point 261-263 °C(lit.)
density 1.083 g/mL at 25 °C(lit.)
refractive index n20/D 1.620(lit.)
Fp >230 °F
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly)
pka5.67(at 20℃)
form Liquid
color Pale Orange
Odorat 100.00 %. burnt oily herbal floral sweet
Odor Typeburnt
Water Solubility Slightly soluble
Sensitive Light Sensitive
Merck 14,5441
BRN 110926
InChIKeyMUDSDYNRBDKLGK-UHFFFAOYSA-N
LogP2.610
CAS DataBase Reference491-35-0(CAS DataBase Reference)
NIST Chemistry ReferenceQuinoline, 4-methyl-(491-35-0)
EPA Substance Registry SystemQuinoline, 4-methyl- (491-35-0)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-68-40
Safety Statements 26-36-45-36/37/39-22
WGK Germany 3
RTECS OH0316000
8-10
TSCA Yes
HS Code 29334900
Hazardous Substances Data491-35-0(Hazardous Substances Data)
MSDS Information
ProviderLanguage
Lepidine English
SigmaAldrich English
ACROS English
ALFA English
4-methylquinoline Usage And Synthesis
DescriptionRefer to 6-METHYLQUINOLINE.
Chemical Propertiesclear slightly yellow to brown liquid
UsesLepidine is used in the preparation of certain dyes.
Uses4-Methylquinoline is used as a reagent in the synthesis of azetidine based ene-amides as potent bacterial enoyl ACP reductase inhibitors. Also used as a reagent in the synthesis of cyanine-styryl dyes with enhanced photostability for fluorescent DNA imaging.
DefinitionChEBI: A methylquinoline carrying a methyl substituent at position 4.
Synthesis Reference(s)Tetrahedron Letters, 28, p. 5291, 1987 DOI: 10.1016/S0040-4039(00)96710-8
General DescriptionSynthesis of lepidine from 4-anilinobutan-2-one in ethanol in the presence of HCl or FeCl3 has been reported. Nitration of lepidine has been reported.
Purification MethodsReflux lepidine with BaO, then fractionally distil it. Further purify it via its recrystallised dichromate salt (m 138o) (from H2O). [Cumper et al. J Chem Soc 1176 1962.] [Beilstein 20 III/IV 3477, 20/7 V 389.]
Lucigenin(bis-N-methylacridiniumnitrate) 2-HYDROXY-4-METHYLQUINOLINE BATHOPHENANTHROLINEDISULFONIC ACID DISODIUM SALT TRIHYDRATE Isoquinoline 2-PHENYL-QUINOLINE-4-CARBOXYLIC ACID METHYL ESTER QUINOLINE-4-CARBOXYLIC ACID 8-Methylquinoline 2,4-DIMETHYLQUINOLINE Quinclorac 2-METHYL-9-ACRIDINECARBALDEHYDE 1,1'-DIETHYL-4,4'-CARBOCYANINE IODIDE Bathophenanthroline Ethoxyquin 8-Hydroxyquinoline CINCHOPHEN 6-Hydroxy-2(1H)-3,4-dihydroquinolinone Quinhydrone Lepidine, 2-chloro-

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