Tert-butyl3-hydroxy-3-[2-(trifluoromethyl)phenyl]azetidine-1-carboxylate CAS 1609671-83-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1609671-83-1
Molecular FormulaC15H18F3NO3
Molecular Weight317.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl3-hydroxy-3-[2-(trifluoromethyl)phenyl]azetidine-1-carboxylate CAS 1609671-83-1 chemical structure

Description

The molecular framework of Tert-butyl3-hydroxy-3-[2-(trifluoromethyl)phenyl]azetidine-1-carboxylate (C15H18F3NO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies Tert-butyl3-hydroxy-3-[2-(trifluoromethyl)phenyl]azetidine-1-carboxylate (CAS 1609671-83-1), a certified reference material (molecular formula C15H18F3NO3, MW 317.30 g/mol) for analytical method development and quality control.

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 Tert-butyl3-hydroxy-3-[2-(trifluoromethyl)phenyl]azetidine-1-carboxylate 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 FormulaC15H18F3NO3
Molecular Weight317.30 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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.)1993
Halogen ContentF-containing
Nitrogen Atoms1

Recommended Standards

Why CATO?