(2S,3R,4R)-3,4-bis(benzyloxy)-2-(iodomethyl)-5-methoxytetrahydrofuran CAS 869476-25-5

Purity 97%+In StockPharmaceutical Standards
CAS No.869476-25-5
Molecular FormulaC20H23IO4
Molecular Weight454.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2S,3R,4R)-3,4-bis(benzyloxy)-2-(iodomethyl)-5-methoxytetrahydrofuran CAS 869476-25-5 chemical structure

Description

(2S,3R,4R)-3,4-bis(benzyloxy)-2-(iodomethyl)-5-methoxytetrahydrofuran (CAS 869476-25-5) is a high-purity analytical reference standard with the molecular formula C20H23IO4 and a molecular weight of 454.30 g/mol.

Based on its molecular formula C20H23IO4, (2S,3R,4R)-3,4-bis(benzyloxy)-2-(iodomethyl)-5-methoxytetrahydrofuran contains a flavonoid core, a hydroxyl group, an ether linkage, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 454.30 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.

CATO manufactures (2S,3R,4R)-3,4-bis(benzyloxy)-2-(iodomethyl)-5-methoxytetrahydrofuran 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 FormulaC20H23IO4
Molecular Weight454.30 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing

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