1-(5-Fluoropyridin-2-yl)-4-oxocyclohexanecarbonitrile CAS 960371-10-2

Purity 97%+In StockPharmaceutical Standards
CAS No.960371-10-2
Molecular FormulaC12H11FN2O
Molecular Weight218.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(5-Fluoropyridin-2-yl)-4-oxocyclohexanecarbonitrile CAS 960371-10-2 chemical structure

Description

As a certified reference material (CRM), 1-(5-Fluoropyridin-2-yl)-4-oxocyclohexanecarbonitrile 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.

1-(5-Fluoropyridin-2-yl)-4-oxocyclohexanecarbonitrile (CAS 960371-10-2), molecular formula C12H11FN2O and molecular weight 218.23 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, 1-(5-Fluoropyridin-2-yl)-4-oxocyclohexanecarbonitrile is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 218.23 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC12H11FN2O
Molecular Weight218.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms2

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