N-((3-(Benzo[d]oxazol-2-yl)phenyl)carbamothioyl)-3-fluorobenzamide CAS 590394-64-2

Purity 97%+In StockPharmaceutical Standards
CAS No.590394-64-2
Molecular FormulaC21H14FN3O2S
Molecular Weight391.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((3-(Benzo[d]oxazol-2-yl)phenyl)carbamothioyl)-3-fluorobenzamide CAS 590394-64-2 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.

N-((3-(Benzo[d]oxazol-2-yl)phenyl)carbamothioyl)-3-fluorobenzamide (CAS 590394-64-2), molecular formula C21H14FN3O2S and molecular weight 391.42 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C21H14FN3O2S, N-((3-(Benzo[d]oxazol-2-yl)phenyl)carbamothioyl)-3-fluorobenzamide contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 391.42 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures N-((3-(Benzo[d]oxazol-2-yl)phenyl)carbamothioyl)-3-fluorobenzamide 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 FormulaC21H14FN3O2S
Molecular Weight391.42 g/mol
Purity97%+
StorageStore at 2-8°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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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