tert-Butyl ((2-bromo-4-methylthiazol-5-yl)methyl)carbamate CAS 2680681-16-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2680681-16-5
Molecular FormulaC10H15BrN2O2S
Molecular Weight307.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl ((2-bromo-4-methylthiazol-5-yl)methyl)carbamate CAS 2680681-16-5 chemical structure

Description

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.

CATO supplies tert-Butyl ((2-bromo-4-methylthiazol-5-yl)methyl)carbamate (CAS 2680681-16-5), a certified reference material (molecular formula C10H15BrN2O2S, MW 307.21 g/mol) for analytical method development and quality control.

The molecular framework of tert-Butyl ((2-bromo-4-methylthiazol-5-yl)methyl)carbamate (C10H15BrN2O2S) 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 its high hydrophobicity (logP), 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).

CATO manufactures tert-Butyl ((2-bromo-4-methylthiazol-5-yl)methyl)carbamate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC10H15BrN2O2S
Molecular Weight307.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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.)2002
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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