Methyl 3-((4-iodophenyl)amino)-3-oxopropanoate CAS 658709-61-6

Purity 97%+In StockPharmaceutical Standards
CAS No.658709-61-6
Molecular FormulaC10H10INO3
Molecular Weight319.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-((4-iodophenyl)amino)-3-oxopropanoate CAS 658709-61-6 chemical structure

Description

Methyl 3-((4-iodophenyl)amino)-3-oxopropanoate (CAS 658709-61-6) is a high-purity analytical reference standard with the molecular formula C10H10INO3 and a molecular weight of 319.10 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution, Methyl 3-((4-iodophenyl)amino)-3-oxopropanoate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 319.10 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 Methyl 3-((4-iodophenyl)amino)-3-oxopropanoate 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 FormulaC10H10INO3
Molecular Weight319.10 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentI-containing
Nitrogen Atoms1

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