Ethyl (E)-5-((allylimino)methyl)-4-chloro-3-methylbenzofuran-2-carboxylate CAS 339285-62-0

Purity 97%+In StockPharmaceutical Standards
CAS No.339285-62-0
Molecular FormulaC16H16ClNO3
Molecular Weight305.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl (E)-5-((allylimino)methyl)-4-chloro-3-methylbenzofuran-2-carboxylate CAS 339285-62-0 chemical structure

Description

CATO manufactures Ethyl (E)-5-((allylimino)methyl)-4-chloro-3-methylbenzofuran-2-carboxylate 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 (E)-5-((allylimino)methyl)-4-chloro-3-methylbenzofuran-2-carboxylate (CAS 339285-62-0), molecular formula C16H16ClNO3 and molecular weight 305.76 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Ethyl (E)-5-((allylimino)methyl)-4-chloro-3-methylbenzofuran-2-carboxylate (C16H16ClNO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC16H16ClNO3
Molecular Weight305.76 g/mol
AppearancePale yellow to 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1

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