5-(3-Fluorophenyl)-1-oxo-1λ4-thiomorpholine-3-carboxylic acid CAS 1560915-38-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1560915-38-9
Molecular FormulaC11H12FNO3S
Molecular Weight257.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3-Fluorophenyl)-1-oxo-1λ4-thiomorpholine-3-carboxylic acid CAS 1560915-38-9 chemical structure

Description

CATO supplies 5-(3-Fluorophenyl)-1-oxo-1λ4-thiomorpholine-3-carboxylic acid (CAS 1560915-38-9), a certified reference material (molecular formula C11H12FNO3S, MW 257.28 g/mol) for analytical method development and quality control.

The molecular framework of 5-(3-Fluorophenyl)-1-oxo-1λ4-thiomorpholine-3-carboxylic acid (C11H12FNO3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine 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. 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 5-(3-Fluorophenyl)-1-oxo-1λ4-thiomorpholine-3-carboxylic acid 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 FormulaC11H12FNO3S
Molecular Weight257.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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