N'-[(1E)-{3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl}methylidene]-3,4,5-trimethoxybenzohydrazide CAS 477886-84-3

Purity 97%+In StockPharmaceutical Standards
CAS No.477886-84-3
Molecular FormulaC21H20ClN3O5S
Molecular Weight461.92 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N'-[(1E)-{3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl}methylidene]-3,4,5-trimethoxybenzohydrazide CAS 477886-84-3 chemical structure

Description

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

N'-[(1E)-{3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl}methylidene]-3,4,5-trimethoxybenzohydrazide (CAS 477886-84-3) is a high-purity analytical reference standard with the molecular formula C21H20ClN3O5S and a molecular weight of 461.92 g/mol.

N'-[(1E)-{3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl}methylidene]-3,4,5-trimethoxybenzohydrazide (C21H20ClN3O5S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC21H20ClN3O5S
Molecular Weight461.92 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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