2-Chloroethyl (5-bromothiazol-2-yl)carbamate CAS 353265-54-0

Purity 97%+In StockPharmaceutical Standards
CAS No.353265-54-0
Molecular FormulaC6H6BrClN2O2S
Molecular Weight285.55 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloroethyl (5-bromothiazol-2-yl)carbamate CAS 353265-54-0 chemical structure

Description

The molecular framework of 2-Chloroethyl (5-bromothiazol-2-yl)carbamate (C6H6BrClN2O2S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, an aromatic ring system. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

2-Chloroethyl (5-bromothiazol-2-yl)carbamate (CAS 353265-54-0) is a high-purity analytical reference standard with the molecular formula C6H6BrClN2O2S and a molecular weight of 285.55 g/mol.

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

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 FormulaC6H6BrClN2O2S
Molecular Weight285.55 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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.)2025
Halogen ContentCl/Br-containing
Nitrogen Atoms2
Sulfur Atoms1

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