(5-(2-Fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone CAS 2070015-36-8

Purity 97%+In StockPharmaceutical Standards
CAS No.2070015-36-8
Molecular FormulaC18H12FIOS
Molecular Weight422.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-(2-Fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone CAS 2070015-36-8 chemical structure

Description

Owing to a steroid core, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine/iodine substitution, (5-(2-Fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 422.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 (5-(2-Fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone (CAS 2070015-36-8), a certified reference material (molecular formula C18H12FIOS, MW 422.26 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.

CATO manufactures (5-(2-Fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)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 FormulaC18H12FIOS
Molecular Weight422.26 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentF/I-containing
Sulfur Atoms1

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