(S)-2-Methoxy-4-(2-trifluoromethyl-pyrrolidin-1-yl)aniline CAS 1416348-84-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1416348-84-9
Molecular FormulaC12H15F3N2O
Molecular Weight260.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-Methoxy-4-(2-trifluoromethyl-pyrrolidin-1-yl)aniline CAS 1416348-84-9 chemical structure

Description

(S)-2-Methoxy-4-(2-trifluoromethyl-pyrrolidin-1-yl)aniline (CAS 1416348-84-9), molecular formula C12H15F3N2O and molecular weight 260.26 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, (S)-2-Methoxy-4-(2-trifluoromethyl-pyrrolidin-1-yl)aniline (C12H15F3N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 260.26 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

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 FormulaC12H15F3N2O
Molecular Weight260.26 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms2

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