Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate CAS 471248-25-6

Purity 97%+In StockPharmaceutical Standards
CAS No.471248-25-6
Molecular FormulaC15H13IO4
Molecular Weight384.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate CAS 471248-25-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 384.17 g/mol gives Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate (CAS 471248-25-6), a certified reference material (molecular formula C15H13IO4, MW 384.17 g/mol) for analytical method development and quality control.

Structurally, Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate (C15H13IO4) contains a flavonoid core, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 384.17 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures Methyl 2-(4-(4-hydroxyphenoxy)-3-iodophenyl)acetate 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 FormulaC15H13IO4
Molecular Weight384.17 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°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; 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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