2-{2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4-yl}acetic acid CAS 1511084-71-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1511084-71-1
Molecular FormulaC11H8Cl2N2O2S
Molecular Weight303.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-{2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4-yl}acetic acid CAS 1511084-71-1 chemical structure

Description

2-{2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4-yl}acetic acid (CAS 1511084-71-1), molecular formula C11H8Cl2N2O2S and molecular weight 303.16 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-{2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4-yl}acetic acid (C11H8Cl2N2O2S) 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. 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.

As a certified reference material (CRM), 2-{2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4-yl}acetic 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 FormulaC11H8Cl2N2O2S
Molecular Weight303.16 g/mol
Purity97%+
StorageStore at 2-8°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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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