(E)-[1-(2,4-Dimethyl-1,3-thiazol-5-yl)ethylidene]amino 3,4-dichlorobenzoate CAS 477872-40-5

Purity 97%+In StockPharmaceutical Standards
CAS No.477872-40-5
Molecular FormulaC14H12Cl2N2O2S
Molecular Weight343.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-[1-(2,4-Dimethyl-1,3-thiazol-5-yl)ethylidene]amino 3,4-dichlorobenzoate CAS 477872-40-5 chemical structure

Description

CATO manufactures (E)-[1-(2,4-Dimethyl-1,3-thiazol-5-yl)ethylidene]amino 3,4-dichlorobenzoate 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.

(E)-[1-(2,4-Dimethyl-1,3-thiazol-5-yl)ethylidene]amino 3,4-dichlorobenzoate (CAS 477872-40-5), molecular formula C14H12Cl2N2O2S and molecular weight 343.23 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (E)-[1-(2,4-Dimethyl-1,3-thiazol-5-yl)ethylidene]amino 3,4-dichlorobenzoate (C14H12Cl2N2O2S) 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).

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

Physical & Chemical Properties

Molecular FormulaC14H12Cl2N2O2S
Molecular Weight343.23 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 ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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