(R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether (R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane 457634-26-3 Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester CAS 457634-26-3

Purity 97%+In StockPharmaceutical Standards
CAS No.457634-26-3
Molecular FormulaC21H25IO4
Molecular Weight468.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether
(R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane
457634-26-3
Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester CAS 457634-26-3 chemical structure

Description

The occurrence of (R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether (R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane 457634-26-3 Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester is closely related to a flavonoid core, a hydroxyl group, an ether linkage, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether (R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane 457634-26-3 Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester (CAS 457634-26-3), molecular formula C21H25IO4 and molecular weight 468.33 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether (R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane 457634-26-3 Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester (C21H25IO4) is characterized by a flavonoid core, 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 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.

As a certified reference material (CRM), (R)-(2-Methyl-4-tert-butylcarbonate)benzene 1-(1-Phenyl-3-iodopropyl) Ether (R)-3-Iodo-1-phenyl-1-[2-methyl-4-[(tert-butoxycarbonyl)-oxy]phenoxy]propane 457634-26-3 Carbonic Acid 1,1-Dimethylethyl 4-[(1R)-3-Iodo-1-phenylpropoxy]-3-methylphenyl Ester meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC21H25IO4
Molecular Weight468.33 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.)2025
Halogen ContentI-containing

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