trans-2-ethoxy-4-[1-(3-iodo-1-bicyclo[1.1.1]pentanyl)-1-methyl-ethyl]tetrahydrofuran CAS 2374231-15-7

Purity 97%+In StockPharmaceutical Standards
CAS No.2374231-15-7
Molecular FormulaC14H23IO2
Molecular Weight350.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-2-ethoxy-4-[1-(3-iodo-1-bicyclo[1.1.1]pentanyl)-1-methyl-ethyl]tetrahydrofuran CAS 2374231-15-7 chemical structure

Description

Structurally, trans-2-ethoxy-4-[1-(3-iodo-1-bicyclo[1.1.1]pentanyl)-1-methyl-ethyl]tetrahydrofuran (C14H23IO2) 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 350.24 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).

CATO supplies trans-2-ethoxy-4-[1-(3-iodo-1-bicyclo[1.1.1]pentanyl)-1-methyl-ethyl]tetrahydrofuran (CAS 2374231-15-7), a certified reference material (molecular formula C14H23IO2, MW 350.24 g/mol) for analytical method development and quality control.

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 FormulaC14H23IO2
Molecular Weight350.24 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1999
Halogen ContentI-containing

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