Methyl 6-fluoro-1-oxoisoindoline-5-carboxylate CAS 1427446-01-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1427446-01-2
Molecular FormulaC10H8FNO3
Molecular Weight209.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 6-fluoro-1-oxoisoindoline-5-carboxylate CAS 1427446-01-2 chemical structure

Description

As a certified reference material (CRM), Methyl 6-fluoro-1-oxoisoindoline-5-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.

Methyl 6-fluoro-1-oxoisoindoline-5-carboxylate (CAS 1427446-01-2), molecular formula C10H8FNO3 and molecular weight 209.17 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C10H8FNO3, Methyl 6-fluoro-1-oxoisoindoline-5-carboxylate 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 209.17 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC10H8FNO3
Molecular Weight209.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-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 methanol, ethanol, DMSO
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms1

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