Methyl 3-(4-bromobenzenesulfonamido)-3-[4-(propan-2-yl)phenyl]propanoate CAS 477858-91-6

Purity 97%+In StockPharmaceutical Standards
CAS No.477858-91-6
Molecular FormulaC19H22BrNO4S
Molecular Weight440.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(4-bromobenzenesulfonamido)-3-[4-(propan-2-yl)phenyl]propanoate CAS 477858-91-6 chemical structure

Description

CATO manufactures Methyl 3-(4-bromobenzenesulfonamido)-3-[4-(propan-2-yl)phenyl]propanoate 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.

CATO supplies Methyl 3-(4-bromobenzenesulfonamido)-3-[4-(propan-2-yl)phenyl]propanoate (CAS 477858-91-6), a certified reference material (molecular formula C19H22BrNO4S, MW 440.35 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 3-(4-bromobenzenesulfonamido)-3-[4-(propan-2-yl)phenyl]propanoate (C19H22BrNO4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC19H22BrNO4S
Molecular Weight440.35 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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