2-Iodo-6,7,8,9-tetrahydro-4H-thieno[2,3-c]chromen-4-one CAS 2839564-11-1

Purity 97%+In StockPharmaceutical Standards
CAS No.2839564-11-1
Molecular FormulaC11H9IO2S
Molecular Weight332.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Iodo-6,7,8,9-tetrahydro-4H-thieno[2,3-c]chromen-4-one CAS 2839564-11-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-Iodo-6,7,8,9-tetrahydro-4H-thieno[2,3-c]chromen-4-one.

2-Iodo-6,7,8,9-tetrahydro-4H-thieno[2,3-c]chromen-4-one (CAS 2839564-11-1), molecular formula C11H9IO2S and molecular weight 332.16 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system, 2-Iodo-6,7,8,9-tetrahydro-4H-thieno[2,3-c]chromen-4-one is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 332.16 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).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H9IO2S
Molecular Weight332.16 g/mol
Purity97%+
StorageStore at 2-8°C, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2003
Halogen ContentI-containing
Sulfur Atoms1

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