6-bromo-4-hydroxy-8-methylquinoline-3-carbonitrile CAS 67643-41-8

Purity 97%+In StockPharmaceutical Standards
CAS No.67643-41-8
Molecular FormulaC11H7BrN2O
Molecular Weight263.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-bromo-4-hydroxy-8-methylquinoline-3-carbonitrile CAS 67643-41-8 chemical structure

Description

The molecular framework of 6-bromo-4-hydroxy-8-methylquinoline-3-carbonitrile (C11H7BrN2O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 6-bromo-4-hydroxy-8-methylquinoline-3-carbonitrile (CAS 67643-41-8), a certified reference material (molecular formula C11H7BrN2O, MW 263.09 g/mol) for analytical method development and quality control.

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.

CATO manufactures 6-bromo-4-hydroxy-8-methylquinoline-3-carbonitrile 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.

Physical & Chemical Properties

Molecular FormulaC11H7BrN2O
Molecular Weight263.09 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentBr-containing
Nitrogen Atoms2

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