Ethyl 5-bromo-2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate CAS 1260664-49-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1260664-49-0
Molecular FormulaC12H16BrNO4S
Molecular Weight350.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-bromo-2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate CAS 1260664-49-0 chemical structure

Description

As a certified reference material (CRM), Ethyl 5-bromo-2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies Ethyl 5-bromo-2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate (CAS 1260664-49-0), a certified reference material (molecular formula C12H16BrNO4S, MW 350.23 g/mol) for analytical method development and quality control.

The molecular framework of Ethyl 5-bromo-2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate (C12H16BrNO4S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC12H16BrNO4S
Molecular Weight350.23 g/mol
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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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