3-((4-(Tert-butyl)benzyl)oxy)-N-(3,4-difluorophenyl)thiophene-2-carboxamide CAS 344270-65-1

Purity 97%+In StockPharmaceutical Standards
CAS No.344270-65-1
Molecular FormulaC22H21F2NO2S
Molecular Weight401.47 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((4-(Tert-butyl)benzyl)oxy)-N-(3,4-difluorophenyl)thiophene-2-carboxamide CAS 344270-65-1 chemical structure

Description

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

3-((4-(Tert-butyl)benzyl)oxy)-N-(3,4-difluorophenyl)thiophene-2-carboxamide (CAS 344270-65-1) is a high-purity analytical reference standard with the molecular formula C22H21F2NO2S and a molecular weight of 401.47 g/mol.

3-((4-(Tert-butyl)benzyl)oxy)-N-(3,4-difluorophenyl)thiophene-2-carboxamide (C22H21F2NO2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. 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.

CATO manufactures 3-((4-(Tert-butyl)benzyl)oxy)-N-(3,4-difluorophenyl)thiophene-2-carboxamide 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 FormulaC22H21F2NO2S
Molecular Weight401.47 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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