4-Chloro-6-(4-(trifluoromethoxy)phenyl)pyrimidine CAS 954221-84-2

Purity 97%+In StockPharmaceutical Standards
CAS No.954221-84-2
Molecular FormulaC11H6ClF3N2O
Molecular Weight274.63 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-6-(4-(trifluoromethoxy)phenyl)pyrimidine CAS 954221-84-2 chemical structure

Description

CATO supplies 4-Chloro-6-(4-(trifluoromethoxy)phenyl)pyrimidine (CAS 954221-84-2), a certified reference material (molecular formula C11H6ClF3N2O, MW 274.63 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H6ClF3N2O, 4-Chloro-6-(4-(trifluoromethoxy)phenyl)pyrimidine contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 274.63 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.

CATO manufactures 4-Chloro-6-(4-(trifluoromethoxy)phenyl)pyrimidine 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.

Physical & Chemical Properties

Molecular FormulaC11H6ClF3N2O
Molecular Weight274.63 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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