4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline CAS 866133-62-2

Purity 97%+In StockPharmaceutical Standards
CAS No.866133-62-2
Molecular FormulaC18H15NOS
Molecular Weight293.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline CAS 866133-62-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 293.38 g/mol gives 4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline (CAS 866133-62-2), molecular formula C18H15NOS and molecular weight 293.38 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline (C18H15NOS) is characterized by a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 4-Methyl-6-phenoxy-2H,3H-thieno[3,2-c]quinoline 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 FormulaC18H15NOS
Molecular Weight293.38 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1
Sulfur Atoms1

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