(Z)-3-iodo-N-[(4-methoxyphenyl)methyl]but-2-enamide CAS 1221589-82-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1221589-82-7
Molecular FormulaC12H20INO2
Molecular Weight337.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-3-iodo-N-[(4-methoxyphenyl)methyl]but-2-enamide CAS 1221589-82-7 chemical structure

Description

CATO manufactures (Z)-3-iodo-N-[(4-methoxyphenyl)methyl]but-2-enamide 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.

CATO supplies (Z)-3-iodo-N-[(4-methoxyphenyl)methyl]but-2-enamide (CAS 1221589-82-7), a certified reference material (molecular formula C12H20INO2, MW 337.20 g/mol) for analytical method development and quality control.

Structurally, (Z)-3-iodo-N-[(4-methoxyphenyl)methyl]but-2-enamide (C12H20INO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 337.20 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC12H20INO2
Molecular Weight337.20 g/mol
AppearanceWhite to pale 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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1990
Halogen ContentI-containing
Nitrogen Atoms1

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