4-(2-((3-(trifluoromethyl)phenyl)amino)thiazol-4-yl)benzene-1,2-diol hydrochloride CAS 1274903-94-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1274903-94-4
Molecular FormulaC16H11F3N2O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2-((3-(trifluoromethyl)phenyl)amino)thiazol-4-yl)benzene-1,2-diol hydrochloride CAS 1274903-94-4 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, 4-(2-((3-(trifluoromethyl)phenyl)amino)thiazol-4-yl)benzene-1,2-diol hydrochloride is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 388.79 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

4-(2-((3-(trifluoromethyl)phenyl)amino)thiazol-4-yl)benzene-1,2-diol hydrochloride (CAS 1274903-94-4), molecular formula C16H11F3N2O2SHCl and molecular weight 388.79 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.

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 FormulaC16H11F3N2O2S HCl
Molecular Weight388.79 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms2
Sulfur Atoms1

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