6-Fluoro-5-iodo-2-methylquinoline CAS 1420789-75-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1420789-75-8
Molecular FormulaC10H7FIN
Molecular Weight287.07 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Fluoro-5-iodo-2-methylquinoline CAS 1420789-75-8 chemical structure

Description

CATO manufactures 6-Fluoro-5-iodo-2-methylquinoline under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

6-Fluoro-5-iodo-2-methylquinoline (CAS 1420789-75-8) is a high-purity analytical reference standard with the molecular formula C10H7FIN and a molecular weight of 287.07 g/mol.

6-Fluoro-5-iodo-2-methylquinoline (C10H7FIN) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC10H7FIN
Molecular Weight287.07 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF/I-containing
Nitrogen Atoms1

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