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Lepidine, 97%, Thermo Scientific Chemicals
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Catalog number A14040.30
also known as A14040-30
Price (USD)/ Each
807.00
-
Quantity:
250 g
Price (USD)/ Each
807.00
Lepidine, 97%, Thermo Scientific Chemicals
Catalog numberA14040.30
Price (USD)/ Each
807.00
-
Chemical Identifiers
CAS491-35-0
IUPAC Name4-methylquinoline
Molecular FormulaC10H9N
InChI KeyMUDSDYNRBDKLGK-UHFFFAOYSA-N
SMILESCC1=C2C=CC=CC2=NC=C1
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Specifications
Specification Sheet
Specification SheetRefractive Index1.6155-1.6205 @ 20?C
FormLiquid
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to yellow
Lepidine is used in the preparation of certain dyes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Lepidine is used in the preparation of certain dyes.
Solubility
Slightly soluble in water.
Notes
Light sensitive. Incompatible with oxidizing agents. Incompatible with oxidizing agents.
Lepidine is used in the preparation of certain dyes.
Solubility
Slightly soluble in water.
Notes
Light sensitive. Incompatible with oxidizing agents. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- K.R.Justin Thomas; Marappan Velusamy; Jiann T.Lin ; Chin-Hsiung Chien; Yu-Tai Tao; Yuh S.Wen; Ya-Hui Hu; Pi-Tai Chou. Efficient red-emitting cyclometalated iridium(III) complexes containing lepidine-based ligands. Inorg. Chem. 2005, 44,(16), 5677-5685
- Martin J.Weiss; Charles R.Hauser. The acylation and carbethoxylation of quinaldine, lepidine and α-picoline using sodium amide or potassium amide. J. Am. Chem. Soc. 1949, 71,(6), 2023-2026.
- Lepidine and similar compounds can be alkylated at the 2-position by free radicals generated by the action of t-butyl hydroperoxide and a salt of Fe(II) on a primary or secondary alkyl iodide: Acta Chem. Scand., 43, 995 (1989). Similarly, 2-formylation can be achieved in high yield using 1,3,5-trioxane in the presence of TFA, t-BuOOH and FeSO4 in acetonitrile: J. Org. Chem., 51, 536 (1986).