tert-Butyl 5-bromo-4-nitrothiophene-2-carboxylate CAS 62224-29-7

Purity 97%+In StockPharmaceutical Standards
CAS No.62224-29-7
Molecular FormulaC9H10BrNO4S
Molecular Weight308.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 5-bromo-4-nitrothiophene-2-carboxylate CAS 62224-29-7 chemical structure

Description

As a certified reference material (CRM), tert-Butyl 5-bromo-4-nitrothiophene-2-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 tert-Butyl 5-bromo-4-nitrothiophene-2-carboxylate (CAS 62224-29-7), a certified reference material (molecular formula C9H10BrNO4S, MW 308.15 g/mol) for analytical method development and quality control.

tert-Butyl 5-bromo-4-nitrothiophene-2-carboxylate (C9H10BrNO4S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC9H10BrNO4S
Molecular Weight308.15 g/mol
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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