Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone CAS 52421-61-1

Purity 97%+In StockPharmaceutical Standards
CAS No.52421-61-1
Molecular FormulaC16H11NOS
Molecular Weight265.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone CAS 52421-61-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone.

Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone (CAS 52421-61-1), molecular formula C16H11NOS and molecular weight 265.33 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 265.33 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.

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.

As a certified reference material (CRM), Phenyl(2-phenyl-1,3-thiazol-5-yl)methanone 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.

Physical & Chemical Properties

Molecular FormulaC16H11NOS
Molecular Weight265.33 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.)1971
Nitrogen Atoms1
Sulfur Atoms1

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Why CATO?