(Z)-3-(2-aminoethyl)-5-(3-bromobenzylidene)thiazolidine-2,4-dione hydrochloride CAS 1049787-18-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1049787-18-9
Molecular FormulaC12H11BrN2O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-3-(2-aminoethyl)-5-(3-bromobenzylidene)thiazolidine-2,4-dione hydrochloride CAS 1049787-18-9 chemical structure

Description

Based on its molecular formula C12H11BrN2O2SHCl, (Z)-3-(2-aminoethyl)-5-(3-bromobenzylidene)thiazolidine-2,4-dione hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 363.65 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

(Z)-3-(2-aminoethyl)-5-(3-bromobenzylidene)thiazolidine-2,4-dione hydrochloride (CAS 1049787-18-9), molecular formula C12H11BrN2O2SHCl and molecular weight 363.65 g/mol, is a CATO reference standard with documented purity and traceability.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), (Z)-3-(2-aminoethyl)-5-(3-bromobenzylidene)thiazolidine-2,4-dione hydrochloride 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 FormulaC12H11BrN2O2S HCl
Molecular Weight363.65 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl/Br-containing
Nitrogen Atoms2
Sulfur Atoms1

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