5-(Furan-2-yl)-3-(4-methoxyphenyl)-4,5-dihydro-1h-pyrazole-1-carbothioamide CAS 394682-47-4

Purity 97%+In StockPharmaceutical Standards
CAS No.394682-47-4
Molecular FormulaC15H15N3O2S
Molecular Weight301.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(Furan-2-yl)-3-(4-methoxyphenyl)-4,5-dihydro-1h-pyrazole-1-carbothioamide CAS 394682-47-4 chemical structure

Description

5-(Furan-2-yl)-3-(4-methoxyphenyl)-4,5-dihydro-1h-pyrazole-1-carbothioamide (CAS 394682-47-4) is a high-purity analytical reference standard with the molecular formula C15H15N3O2S and a molecular weight of 301.36 g/mol.

The molecular framework of 5-(Furan-2-yl)-3-(4-methoxyphenyl)-4,5-dihydro-1h-pyrazole-1-carbothioamide (C15H15N3O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC15H15N3O2S
Molecular Weight301.36 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3
Sulfur Atoms1

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