ethyl 1-(iodomethyl)-3-thiazol-4-yl-2-oxabicyclo[2.2.2]octane-4-carboxylate CAS 2703779-92-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2703779-92-2
Molecular FormulaC14H18INO3S
Molecular Weight407.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

ethyl 1-(iodomethyl)-3-thiazol-4-yl-2-oxabicyclo[2.2.2]octane-4-carboxylate CAS 2703779-92-2 chemical structure

Description

The molecular framework of ethyl 1-(iodomethyl)-3-thiazol-4-yl-2-oxabicyclo[2.2.2]octane-4-carboxylate (C14H18INO3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

ethyl 1-(iodomethyl)-3-thiazol-4-yl-2-oxabicyclo[2.2.2]octane-4-carboxylate (CAS 2703779-92-2), molecular formula C14H18INO3S and molecular weight 407.27 g/mol, is a CATO reference standard with documented purity and traceability.

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-thiazol-4-yl-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 FormulaC14H18INO3S
Molecular Weight407.27 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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