N-(4-Bromophenyl)-2-(3-oxo-2,3,5,6-tetrahydroimidazo[2,1-b]thiazol-2-yl)acetamide CAS 496011-33-7

Purity 97%+In StockPharmaceutical Standards
CAS No.496011-33-7
Molecular FormulaC13H12BrN3O2S
Molecular Weight354.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Bromophenyl)-2-(3-oxo-2,3,5,6-tetrahydroimidazo[2,1-b]thiazol-2-yl)acetamide CAS 496011-33-7 chemical structure

Description

As a certified reference material (CRM), N-(4-Bromophenyl)-2-(3-oxo-2,3,5,6-tetrahydroimidazo[2,1-b]thiazol-2-yl)acetamide 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.

CATO supplies N-(4-Bromophenyl)-2-(3-oxo-2,3,5,6-tetrahydroimidazo[2,1-b]thiazol-2-yl)acetamide (CAS 496011-33-7), a certified reference material (molecular formula C13H12BrN3O2S, MW 354.22 g/mol) for analytical method development and quality control.

Structurally, N-(4-Bromophenyl)-2-(3-oxo-2,3,5,6-tetrahydroimidazo[2,1-b]thiazol-2-yl)acetamide (C13H12BrN3O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 354.22 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC13H12BrN3O2S
Molecular Weight354.22 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms3
Sulfur Atoms1

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