tert-Butyl 4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate, 97% CAS 732275-91-1

Purity 97%+In StockPharmaceutical Standards
CAS No.732275-91-1
Molecular FormulaC17H22F3NO2
Molecular Weight329.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate, 97% CAS 732275-91-1 chemical structure

Description

CATO manufactures tert-Butyl 4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate, 97% 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 tert-Butyl 4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate, 97% (CAS 732275-91-1), a certified reference material (molecular formula C17H22F3NO2, MW 329.36 g/mol) for analytical method development and quality control.

Structurally, tert-Butyl 4-(4-(trifluoromethyl)phenyl)piperidine-1-carboxylate, 97% (C17H22F3NO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 329.36 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC17H22F3NO2
Molecular Weight329.36 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing
Nitrogen Atoms1

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