Methyl 2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxylate CAS 36701-90-3

Purity 97%+In StockPharmaceutical Standards
CAS No.36701-90-3
Molecular FormulaC14H10F3NO3
Molecular Weight297.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxylate CAS 36701-90-3 chemical structure

Description

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

CATO supplies Methyl 2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxylate (CAS 36701-90-3), a certified reference material (molecular formula C14H10F3NO3, MW 297.23 g/mol) for analytical method development and quality control.

Based on its molecular formula C14H10F3NO3, Methyl 2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 297.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC14H10F3NO3
Molecular Weight297.23 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1967
Halogen ContentF-containing
Nitrogen Atoms1

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