2-Fluoro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide CAS 690246-27-6

Purity 97%+In StockPharmaceutical Standards
CAS No.690246-27-6
Molecular FormulaC15H10FN3OS
Molecular Weight299.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Fluoro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide CAS 690246-27-6 chemical structure

Description

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 supplies 2-Fluoro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide (CAS 690246-27-6), a certified reference material (molecular formula C15H10FN3OS, MW 299.32 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution, 2-Fluoro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 299.32 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 2-Fluoro-N-(3-phenyl-1,2,4-thiadiazol-5-yl)benzamide 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 FormulaC15H10FN3OS
Molecular Weight299.32 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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