4-(4-Chlorophenyl)-2,3-dihydro-1,5-benzothiazepine-2-carboxylic Acid CAS 116274-72-7

Purity 97%+In StockPharmaceutical Standards
CAS No.116274-72-7
Molecular FormulaC16H12ClNO2S
Molecular Weight317.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Chlorophenyl)-2,3-dihydro-1,5-benzothiazepine-2-carboxylic Acid CAS 116274-72-7 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 4-(4-Chlorophenyl)-2,3-dihydro-1,5-benzothiazepine-2-carboxylic Acid (CAS 116274-72-7), a certified reference material (molecular formula C16H12ClNO2S, MW 317.79 g/mol) for analytical method development and quality control.

The molecular framework of 4-(4-Chlorophenyl)-2,3-dihydro-1,5-benzothiazepine-2-carboxylic Acid (C16H12ClNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), 4-(4-Chlorophenyl)-2,3-dihydro-1,5-benzothiazepine-2-carboxylic Acid 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 FormulaC16H12ClNO2S
Molecular Weight317.79 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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