4-chloro-N-(2-methoxy-1-methylethyl)-3-nitrobenzenesulfonamide CAS 747412-35-7

Purity 97%+In StockPharmaceutical Standards
CAS No.747412-35-7
Molecular FormulaC10H13ClN2O5S
Molecular Weight308.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-chloro-N-(2-methoxy-1-methylethyl)-3-nitrobenzenesulfonamide CAS 747412-35-7 chemical structure

Description

CATO supplies 4-chloro-N-(2-methoxy-1-methylethyl)-3-nitrobenzenesulfonamide (CAS 747412-35-7), a certified reference material (molecular formula C10H13ClN2O5S, MW 308.74 g/mol) for analytical method development and quality control.

Structurally, 4-chloro-N-(2-methoxy-1-methylethyl)-3-nitrobenzenesulfonamide (C10H13ClN2O5S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 308.74 g/mol, it falls into the moderately-high-molecular-weight range. 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.

As a certified reference material (CRM), 4-chloro-N-(2-methoxy-1-methylethyl)-3-nitrobenzenesulfonamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H13ClN2O5S
Molecular Weight308.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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