Methyl 3-(5-methyl-1-phenyl-1H-pyrazole-4-carboxamido)thiophene-2-carboxylate CAS 321574-08-7

Purity 97%+In StockPharmaceutical Standards
CAS No.321574-08-7
Molecular FormulaC17H15N3O3S
Molecular Weight341.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(5-methyl-1-phenyl-1H-pyrazole-4-carboxamido)thiophene-2-carboxylate CAS 321574-08-7 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.

CATO supplies Methyl 3-(5-methyl-1-phenyl-1H-pyrazole-4-carboxamido)thiophene-2-carboxylate (CAS 321574-08-7), a certified reference material (molecular formula C17H15N3O3S, MW 341.38 g/mol) for analytical method development and quality control.

Based on its molecular formula C17H15N3O3S, Methyl 3-(5-methyl-1-phenyl-1H-pyrazole-4-carboxamido)thiophene-2-carboxylate contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 341.38 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).

CATO manufactures Methyl 3-(5-methyl-1-phenyl-1H-pyrazole-4-carboxamido)thiophene-2-carboxylate 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 FormulaC17H15N3O3S
Molecular Weight341.38 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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3
Sulfur Atoms1

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