(1,3-Thiazol-5-yl)methyl N-(4-chlorophenyl)carbamate CAS 338981-77-4

Purity 97%+In StockPharmaceutical Standards
CAS No.338981-77-4
Molecular FormulaC11H9ClN2O2S
Molecular Weight268.72 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1,3-Thiazol-5-yl)methyl N-(4-chlorophenyl)carbamate CAS 338981-77-4 chemical structure

Description

CATO supplies (1,3-Thiazol-5-yl)methyl N-(4-chlorophenyl)carbamate (CAS 338981-77-4), a certified reference material (molecular formula C11H9ClN2O2S, MW 268.72 g/mol) for analytical method development and quality control.

The molecular framework of (1,3-Thiazol-5-yl)methyl N-(4-chlorophenyl)carbamate (C11H9ClN2O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

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 FormulaC11H9ClN2O2S
Molecular Weight268.72 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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