trans-4-(2-(3-Fluorophenyl)-2-oxoethyl)cyclohexanecarboxylic acid CAS 736136-54-2

Purity 97%+In StockPharmaceutical Standards
CAS No.736136-54-2
Molecular FormulaC15H17FO3
Molecular Weight264.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-4-(2-(3-Fluorophenyl)-2-oxoethyl)cyclohexanecarboxylic acid CAS 736136-54-2 chemical structure

Description

The molecular framework of trans-4-(2-(3-Fluorophenyl)-2-oxoethyl)cyclohexanecarboxylic acid (C15H17FO3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, a polycyclic aromatic system. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

trans-4-(2-(3-Fluorophenyl)-2-oxoethyl)cyclohexanecarboxylic acid (CAS 736136-54-2) is a high-purity analytical reference standard with the molecular formula C15H17FO3 and a molecular weight of 264.29 g/mol.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC15H17FO3
Molecular Weight264.29 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing

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