N-(4,6-bis(4-(tert-butyl)phenoxy)pyrimidin-2-yl)-4-methoxybenzenesulfonamide CAS 866154-37-2

Purity 97%+In StockPharmaceutical Standards
CAS No.866154-37-2
Molecular FormulaC31H35N3O5S
Molecular Weight561.69 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4,6-bis(4-(tert-butyl)phenoxy)pyrimidin-2-yl)-4-methoxybenzenesulfonamide CAS 866154-37-2 chemical structure

Description

CATO supplies N-(4,6-bis(4-(tert-butyl)phenoxy)pyrimidin-2-yl)-4-methoxybenzenesulfonamide (CAS 866154-37-2), a certified reference material (molecular formula C31H35N3O5S, MW 561.69 g/mol) for analytical method development and quality control.

Based on its molecular formula C31H35N3O5S, N-(4,6-bis(4-(tert-butyl)phenoxy)pyrimidin-2-yl)-4-methoxybenzenesulfonamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 561.69 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC31H35N3O5S
Molecular Weight561.69 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
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3
Sulfur Atoms1

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