N-(6-Sulfanylpyridazin-3-yl)furan-2-carboxamide CAS 1286719-94-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1286719-94-5
Molecular FormulaC9H7N3O2S
Molecular Weight221.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(6-Sulfanylpyridazin-3-yl)furan-2-carboxamide CAS 1286719-94-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(6-Sulfanylpyridazin-3-yl)furan-2-carboxamide.

N-(6-Sulfanylpyridazin-3-yl)furan-2-carboxamide (CAS 1286719-94-5) is a high-purity analytical reference standard with the molecular formula C9H7N3O2S and a molecular weight of 221.24 g/mol.

N-(6-Sulfanylpyridazin-3-yl)furan-2-carboxamide (C9H7N3O2S) 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(6-Sulfanylpyridazin-3-yl)furan-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 FormulaC9H7N3O2S
Molecular Weight221.24 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms3
Sulfur Atoms1

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