ethyl 1-(iodomethyl)-3-isopropyl-2-oxabicyclo[2.2.2]octane-4-carboxylate CAS 2731009-91-7

Purity 97%+In StockPharmaceutical Standards
CAS No.2731009-91-7
Molecular FormulaC14H23IO3
Molecular Weight366.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

ethyl 1-(iodomethyl)-3-isopropyl-2-oxabicyclo[2.2.2]octane-4-carboxylate CAS 2731009-91-7 chemical structure

Description

Structurally, ethyl 1-(iodomethyl)-3-isopropyl-2-oxabicyclo[2.2.2]octane-4-carboxylate (C14H23IO3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 366.24 g/mol, it falls into the moderately-high-molecular-weight range. 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).

ethyl 1-(iodomethyl)-3-isopropyl-2-oxabicyclo[2.2.2]octane-4-carboxylate (CAS 2731009-91-7) is a high-purity analytical reference standard with the molecular formula C14H23IO3 and a molecular weight of 366.24 g/mol.

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.

CATO manufactures ethyl 1-(iodomethyl)-3-isopropyl-2-oxabicyclo[2.2.2]octane-4-carboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC14H23IO3
Molecular Weight366.24 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, 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.)2002
Halogen ContentI-containing

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