Ethyl 2-amino-2-(3-bromo-4-methoxyphenyl)acetate hydrochloride CAS 1432677-66-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1432677-66-1
Molecular FormulaC11H14BrNO3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 2-amino-2-(3-bromo-4-methoxyphenyl)acetate hydrochloride CAS 1432677-66-1 chemical structure

Description

CATO supplies Ethyl 2-amino-2-(3-bromo-4-methoxyphenyl)acetate hydrochloride (CAS 1432677-66-1), a certified reference material (molecular formula C11H14BrNO3HCl, MW 324.60 g/mol) for analytical method development and quality control.

The molecular framework of Ethyl 2-amino-2-(3-bromo-4-methoxyphenyl)acetate hydrochloride (C11H14BrNO3HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine 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. 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.

CATO manufactures Ethyl 2-amino-2-(3-bromo-4-methoxyphenyl)acetate hydrochloride 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 FormulaC11H14BrNO3 HCl
Molecular Weight324.60 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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