Tert-butyl (S)-4-(3-bromophenyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide CAS 1379546-88-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1379546-88-9
Molecular FormulaC13H16BrNO5S
Molecular Weight378.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (S)-4-(3-bromophenyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide CAS 1379546-88-9 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.

Tert-butyl (S)-4-(3-bromophenyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide (CAS 1379546-88-9) is a high-purity analytical reference standard with the molecular formula C13H16BrNO5S and a molecular weight of 378.24 g/mol.

Based on its molecular formula C13H16BrNO5S, Tert-butyl (S)-4-(3-bromophenyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 378.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC13H16BrNO5S
Molecular Weight378.24 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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