4'-(Tert-butyl)-3-fluoro-[1,1'-biphenyl]-4-carboxylic acid CAS 926236-47-7

Purity 97%+In StockPharmaceutical Standards
CAS No.926236-47-7
Molecular FormulaC17H17FO2
Molecular Weight272.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4'-(Tert-butyl)-3-fluoro-[1,1'-biphenyl]-4-carboxylic acid CAS 926236-47-7 chemical structure

Description

CATO supplies 4'-(Tert-butyl)-3-fluoro-[1,1'-biphenyl]-4-carboxylic acid (CAS 926236-47-7), a certified reference material (molecular formula C17H17FO2, MW 272.31 g/mol) for analytical method development and quality control.

The molecular framework of 4'-(Tert-butyl)-3-fluoro-[1,1'-biphenyl]-4-carboxylic acid (C17H17FO2) is characterized by a steroid core, 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.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 4'-(Tert-butyl)-3-fluoro-[1,1'-biphenyl]-4-carboxylic 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 FormulaC17H17FO2
Molecular Weight272.31 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing

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