1,3-Dimethyl-N-phenyl-5-((3-(trifluoromethyl)phenyl)thio)-1H-pyrazole-4-carboxamide CAS 158712-48-2

Purity 97%+In StockPharmaceutical Standards
CAS No.158712-48-2
Molecular FormulaC19H16F3N3OS
Molecular Weight391.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,3-Dimethyl-N-phenyl-5-((3-(trifluoromethyl)phenyl)thio)-1H-pyrazole-4-carboxamide CAS 158712-48-2 chemical structure

Description

Based on its molecular formula C19H16F3N3OS, 1,3-Dimethyl-N-phenyl-5-((3-(trifluoromethyl)phenyl)thio)-1H-pyrazole-4-carboxamide contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 391.41 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).

1,3-Dimethyl-N-phenyl-5-((3-(trifluoromethyl)phenyl)thio)-1H-pyrazole-4-carboxamide (CAS 158712-48-2), molecular formula C19H16F3N3OS and molecular weight 391.41 g/mol, is a CATO reference standard with documented purity and traceability.

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 1,3-Dimethyl-N-phenyl-5-((3-(trifluoromethyl)phenyl)thio)-1H-pyrazole-4-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 FormulaC19H16F3N3OS
Molecular Weight391.41 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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