Ethyl 2-(3-chloro-4-ethoxyphenyl)-2-oxoacetate CAS 1443324-59-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1443324-59-1
Molecular FormulaC12H13ClO4
Molecular Weight256.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 2-(3-chloro-4-ethoxyphenyl)-2-oxoacetate CAS 1443324-59-1 chemical structure

Description

CATO manufactures Ethyl 2-(3-chloro-4-ethoxyphenyl)-2-oxoacetate 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.

Ethyl 2-(3-chloro-4-ethoxyphenyl)-2-oxoacetate (CAS 1443324-59-1) is a high-purity analytical reference standard with the molecular formula C12H13ClO4 and a molecular weight of 256.68 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system, Ethyl 2-(3-chloro-4-ethoxyphenyl)-2-oxoacetate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 256.68 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC12H13ClO4
Molecular Weight256.68 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, keep tightly closed to prevent evaporation
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentCl-containing

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