6-iodo-2-(4-(methylamino)phenyl)-4H-chromen-4-one CAS 871101-30-3

Purity 97%+In StockPharmaceutical Standards
CAS No.871101-30-3
Molecular FormulaC16H12INO2
Molecular Weight377.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-iodo-2-(4-(methylamino)phenyl)-4H-chromen-4-one CAS 871101-30-3 chemical structure

Description

CATO manufactures 6-iodo-2-(4-(methylamino)phenyl)-4H-chromen-4-one 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.

6-iodo-2-(4-(methylamino)phenyl)-4H-chromen-4-one (CAS 871101-30-3), molecular formula C16H12INO2 and molecular weight 377.18 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution, 6-iodo-2-(4-(methylamino)phenyl)-4H-chromen-4-one is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 377.18 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC16H12INO2
Molecular Weight377.18 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Nitrogen Atoms1

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