N-((1,1-Dioxidotetrahydrothiophen-3-yl)carbamothioyl)thiophene-2-carboxamide CAS 431066-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.431066-85-2
Molecular FormulaC10H12N2O3S3
Molecular Weight304.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((1,1-Dioxidotetrahydrothiophen-3-yl)carbamothioyl)thiophene-2-carboxamide CAS 431066-85-2 chemical structure

Description

N-((1,1-Dioxidotetrahydrothiophen-3-yl)carbamothioyl)thiophene-2-carboxamide (C10H12N2O3S3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

N-((1,1-Dioxidotetrahydrothiophen-3-yl)carbamothioyl)thiophene-2-carboxamide (CAS 431066-85-2) is a high-purity analytical reference standard with the molecular formula C10H12N2O3S3 and a molecular weight of 304.41 g/mol.

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

As a certified reference material (CRM), N-((1,1-Dioxidotetrahydrothiophen-3-yl)carbamothioyl)thiophene-2-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H12N2O3S3
Molecular Weight304.41 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2
Sulfur Atoms3

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