3-(4-Bromophenyl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide CAS 36104-03-7

Purity 97%+In StockPharmaceutical Standards
CAS No.36104-03-7
Molecular FormulaC11H9BrN2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Bromophenyl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide CAS 36104-03-7 chemical structure

Description

Based on its molecular formula C11H9BrN2SHBr, 3-(4-Bromophenyl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 362.08 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

3-(4-Bromophenyl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide (CAS 36104-03-7), molecular formula C11H9BrN2SHBr and molecular weight 362.08 g/mol, is a CATO reference standard with documented purity and traceability.

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 manufactures 3-(4-Bromophenyl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H9BrN2S HBr
Molecular Weight362.08 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1967
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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