N-(3-Bromo-4-cyclopropoxyphenyl)methanesulfonamide CAS 1243466-39-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1243466-39-8
Molecular FormulaC10H12BrNO3S
Molecular Weight306.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Bromo-4-cyclopropoxyphenyl)methanesulfonamide CAS 1243466-39-8 chemical structure

Description

N-(3-Bromo-4-cyclopropoxyphenyl)methanesulfonamide (CAS 1243466-39-8) is a high-purity analytical reference standard with the molecular formula C10H12BrNO3S and a molecular weight of 306.18 g/mol.

N-(3-Bromo-4-cyclopropoxyphenyl)methanesulfonamide (C10H12BrNO3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

CATO manufactures N-(3-Bromo-4-cyclopropoxyphenyl)methanesulfonamide 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.

Physical & Chemical Properties

Molecular FormulaC10H12BrNO3S
Molecular Weight306.18 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.)1990
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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