phenyl 6-fluoronaphthalene-2-carboxylate CAS 112058-13-6

Purity 97%+In StockPharmaceutical Standards
CAS No.112058-13-6
Molecular FormulaC17H27FO2
Molecular Weight282.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

phenyl 6-fluoronaphthalene-2-carboxylate CAS 112058-13-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 282.39 g/mol gives phenyl 6-fluoronaphthalene-2-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies phenyl 6-fluoronaphthalene-2-carboxylate (CAS 112058-13-6), a certified reference material (molecular formula C17H27FO2, MW 282.39 g/mol) for analytical method development and quality control.

Owing to a steroid core, a hydroxyl group, an ether linkage, fluorine substitution, phenyl 6-fluoronaphthalene-2-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 282.39 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

As a certified reference material (CRM), phenyl 6-fluoronaphthalene-2-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC17H27FO2
Molecular Weight282.39 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing

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