Ethyl (R)-3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate CAS 1047975-40-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1047975-40-5
Molecular FormulaC16H22BrNO4
Molecular Weight372.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl (R)-3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate CAS 1047975-40-5 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies Ethyl (R)-3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate (CAS 1047975-40-5), a certified reference material (molecular formula C16H22BrNO4, MW 372.25 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H22BrNO4, Ethyl (R)-3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 372.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H22BrNO4
Molecular Weight372.25 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
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms1

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