3-((tert-Butoxycarbonyl)amino)-4-(trifluoromethyl)benzoic acid CAS 2287343-68-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2287343-68-2
Molecular FormulaC13H14F3NO4
Molecular Weight305.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((tert-Butoxycarbonyl)amino)-4-(trifluoromethyl)benzoic acid CAS 2287343-68-2 chemical structure

Description

Based on its molecular formula C13H14F3NO4, 3-((tert-Butoxycarbonyl)amino)-4-(trifluoromethyl)benzoic acid 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 305.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 3-((tert-Butoxycarbonyl)amino)-4-(trifluoromethyl)benzoic acid (CAS 2287343-68-2), a certified reference material (molecular formula C13H14F3NO4, MW 305.25 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 3-((tert-Butoxycarbonyl)amino)-4-(trifluoromethyl)benzoic acid 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 FormulaC13H14F3NO4
Molecular Weight305.25 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 methanol, acetonitrile, DMSO, water (slightly soluble)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentF-containing
Nitrogen Atoms1

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