N-((4-((3-(Trifluoromethyl)phenyl)amino)pyridin-3-yl)sulfonyl)propionamide CAS 52157-91-2

Purity 97%+In StockPharmaceutical Standards
CAS No.52157-91-2
Molecular FormulaC15H14F3N3O3S
Molecular Weight373.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((4-((3-(Trifluoromethyl)phenyl)amino)pyridin-3-yl)sulfonyl)propionamide CAS 52157-91-2 chemical structure

Description

Structurally, N-((4-((3-(Trifluoromethyl)phenyl)amino)pyridin-3-yl)sulfonyl)propionamide (C15H14F3N3O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 373.35 g/mol, it falls into the moderately-high-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.

N-((4-((3-(Trifluoromethyl)phenyl)amino)pyridin-3-yl)sulfonyl)propionamide (CAS 52157-91-2), molecular formula C15H14F3N3O3S and molecular weight 373.35 g/mol, is a CATO reference standard with documented purity and traceability.

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 N-((4-((3-(Trifluoromethyl)phenyl)amino)pyridin-3-yl)sulfonyl)propionamide 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 FormulaC15H14F3N3O3S
Molecular Weight373.35 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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