(5-(1,3-Dioxolan-2-yl)thiophen-2-yl)(2-iodophenyl)methanone CAS 898778-10-4

Purity 97%+In StockPharmaceutical Standards
CAS No.898778-10-4
Molecular FormulaC14H11IO3S
Molecular Weight386.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-(1,3-Dioxolan-2-yl)thiophen-2-yl)(2-iodophenyl)methanone CAS 898778-10-4 chemical structure

Description

CATO supplies (5-(1,3-Dioxolan-2-yl)thiophen-2-yl)(2-iodophenyl)methanone (CAS 898778-10-4), a certified reference material (molecular formula C14H11IO3S, MW 386.20 g/mol) for analytical method development and quality control.

The molecular framework of (5-(1,3-Dioxolan-2-yl)thiophen-2-yl)(2-iodophenyl)methanone (C14H11IO3S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, a polycyclic aromatic system. 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 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 (5-(1,3-Dioxolan-2-yl)thiophen-2-yl)(2-iodophenyl)methanone 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 FormulaC14H11IO3S
Molecular Weight386.20 g/mol
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; Hygroscopic; reseal immediately after opening; 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
Sulfur Atoms1

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