methyl 1-(iodomethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylate CAS 2169203-05-6

Purity 97%+In StockPharmaceutical Standards
CAS No.2169203-05-6
Molecular FormulaC8H11IO3
Molecular Weight282.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

methyl 1-(iodomethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylate CAS 2169203-05-6 chemical structure

Description

CATO supplies methyl 1-(iodomethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylate (CAS 2169203-05-6), a certified reference material (molecular formula C8H11IO3, MW 282.08 g/mol) for analytical method development and quality control.

Based on its molecular formula C8H11IO3, methyl 1-(iodomethyl)-2-oxabicyclo[2.1.1]hexane-4-carboxylate contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 282.08 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

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 FormulaC8H11IO3
Molecular Weight282.08 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1998
Halogen ContentI-containing

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