2,2,2-Trifluoroethyl (4-(pyridin-3-yl)thiazol-2-yl)carbamate CAS 1311316-76-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1311316-76-3
Molecular FormulaC11H8F3N3O2S
Molecular Weight303.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,2-Trifluoroethyl (4-(pyridin-3-yl)thiazol-2-yl)carbamate CAS 1311316-76-3 chemical structure

Description

CATO manufactures 2,2,2-Trifluoroethyl (4-(pyridin-3-yl)thiazol-2-yl)carbamate 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 2,2,2-Trifluoroethyl (4-(pyridin-3-yl)thiazol-2-yl)carbamate (CAS 1311316-76-3), a certified reference material (molecular formula C11H8F3N3O2S, MW 303.26 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H8F3N3O2S, 2,2,2-Trifluoroethyl (4-(pyridin-3-yl)thiazol-2-yl)carbamate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 303.26 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC11H8F3N3O2S
Molecular Weight303.26 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.)1990
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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