3-Iodo-6,7-dimethoxy-1-methylquinolin-4(1H)-one CAS 2111895-17-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2111895-17-9
Molecular FormulaC12H12INO3
Molecular Weight345.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Iodo-6,7-dimethoxy-1-methylquinolin-4(1H)-one CAS 2111895-17-9 chemical structure

Description

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.

3-Iodo-6,7-dimethoxy-1-methylquinolin-4(1H)-one (CAS 2111895-17-9) is a high-purity analytical reference standard with the molecular formula C12H12INO3 and a molecular weight of 345.13 g/mol.

Structurally, 3-Iodo-6,7-dimethoxy-1-methylquinolin-4(1H)-one (C12H12INO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 345.13 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.

Physical & Chemical Properties

Molecular FormulaC12H12INO3
Molecular Weight345.13 g/mol
AppearanceOff-white to pale 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; Hygroscopic; reseal immediately after opening; 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.)1997
Halogen ContentI-containing
Nitrogen Atoms1

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