{4-[(4-chlorophenyl)sulfanyl]-3-nitrophenyl}methyl N-cyclohexylcarbamate CAS 320424-17-7

Purity 97%+In StockPharmaceutical Standards
CAS No.320424-17-7
Molecular FormulaC20H21ClN2O4S
Molecular Weight420.91 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

{4-[(4-chlorophenyl)sulfanyl]-3-nitrophenyl}methyl N-cyclohexylcarbamate CAS 320424-17-7 chemical structure

Description

CATO manufactures {4-[(4-chlorophenyl)sulfanyl]-3-nitrophenyl}methyl N-cyclohexylcarbamate 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.

{4-[(4-chlorophenyl)sulfanyl]-3-nitrophenyl}methyl N-cyclohexylcarbamate (CAS 320424-17-7) is a high-purity analytical reference standard with the molecular formula C20H21ClN2O4S and a molecular weight of 420.91 g/mol.

{4-[(4-chlorophenyl)sulfanyl]-3-nitrophenyl}methyl N-cyclohexylcarbamate (C20H21ClN2O4S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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.

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.

Physical & Chemical Properties

Molecular FormulaC20H21ClN2O4S
Molecular Weight420.91 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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