5-(4-Fluorophenyl)-3-(trifluoromethyl)pyridine-2-thiol CAS 1214340-84-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1214340-84-7
Molecular FormulaC12H7F4NS
Molecular Weight273.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(4-Fluorophenyl)-3-(trifluoromethyl)pyridine-2-thiol CAS 1214340-84-7 chemical structure

Description

As a certified reference material (CRM), 5-(4-Fluorophenyl)-3-(trifluoromethyl)pyridine-2-thiol meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies 5-(4-Fluorophenyl)-3-(trifluoromethyl)pyridine-2-thiol (CAS 1214340-84-7), a certified reference material (molecular formula C12H7F4NS, MW 273.25 g/mol) for analytical method development and quality control.

The molecular framework of 5-(4-Fluorophenyl)-3-(trifluoromethyl)pyridine-2-thiol (C12H7F4NS) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, 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.

Physical & Chemical Properties

Molecular FormulaC12H7F4NS
Molecular Weight273.25 g/mol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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