4-(Benzenesulfonyl)-5-(3,4-dichlorophenyl)-1-phenyl-1H-pyrazole CAS 318951-72-3

Purity 97%+In StockPharmaceutical Standards
CAS No.318951-72-3
Molecular FormulaC21H14Cl2N2O2S
Molecular Weight429.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Benzenesulfonyl)-5-(3,4-dichlorophenyl)-1-phenyl-1H-pyrazole CAS 318951-72-3 chemical structure

Description

CATO supplies 4-(Benzenesulfonyl)-5-(3,4-dichlorophenyl)-1-phenyl-1H-pyrazole (CAS 318951-72-3), a certified reference material (molecular formula C21H14Cl2N2O2S, MW 429.32 g/mol) for analytical method development and quality control.

Structurally, 4-(Benzenesulfonyl)-5-(3,4-dichlorophenyl)-1-phenyl-1H-pyrazole (C21H14Cl2N2O2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 15.0, corresponding to approximately 15 ring(s) or double-bond equivalent(s). With a molecular weight of 429.32 g/mol, it falls into the moderately-high-molecular-weight range. 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), 4-(Benzenesulfonyl)-5-(3,4-dichlorophenyl)-1-phenyl-1H-pyrazole 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 FormulaC21H14Cl2N2O2S
Molecular Weight429.32 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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