(5-(4-Fluorophenyl)-3-(prop-2-yn-1-ylthio)-1H-1,2,4-triazol-1-yl)(thiophen-2-yl)methanone CAS 1024198-99-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1024198-99-9
Molecular FormulaC16H10FN3OS2
Molecular Weight343.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-(4-Fluorophenyl)-3-(prop-2-yn-1-ylthio)-1H-1,2,4-triazol-1-yl)(thiophen-2-yl)methanone CAS 1024198-99-9 chemical structure

Description

CATO supplies (5-(4-Fluorophenyl)-3-(prop-2-yn-1-ylthio)-1H-1,2,4-triazol-1-yl)(thiophen-2-yl)methanone (CAS 1024198-99-9), a certified reference material (molecular formula C16H10FN3OS2, MW 343.40 g/mol) for analytical method development and quality control.

The molecular framework of (5-(4-Fluorophenyl)-3-(prop-2-yn-1-ylthio)-1H-1,2,4-triazol-1-yl)(thiophen-2-yl)methanone (C16H10FN3OS2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H10FN3OS2
Molecular Weight343.40 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms2

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