Ethyl 4-amino-2-thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydrothiazole-5-carboxylate CAS 312922-28-4

Purity 97%+In StockPharmaceutical Standards
CAS No.312922-28-4
Molecular FormulaC13H11F3N2O2S2
Molecular Weight348.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 4-amino-2-thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydrothiazole-5-carboxylate CAS 312922-28-4 chemical structure

Description

CATO manufactures Ethyl 4-amino-2-thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydrothiazole-5-carboxylate 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.

CATO supplies Ethyl 4-amino-2-thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydrothiazole-5-carboxylate (CAS 312922-28-4), a certified reference material (molecular formula C13H11F3N2O2S2, MW 348.36 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, Ethyl 4-amino-2-thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydrothiazole-5-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 348.36 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC13H11F3N2O2S2
Molecular Weight348.36 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms2

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