3-((2-Fluorobenzyl)thio)-6-phenylpyridazine CAS 872630-31-4

Purity 97%+In StockPharmaceutical Standards
CAS No.872630-31-4
Molecular FormulaC17H13FN2S
Molecular Weight296.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((2-Fluorobenzyl)thio)-6-phenylpyridazine CAS 872630-31-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 296.36 g/mol gives 3-((2-Fluorobenzyl)thio)-6-phenylpyridazine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-((2-Fluorobenzyl)thio)-6-phenylpyridazine (CAS 872630-31-4), a certified reference material (molecular formula C17H13FN2S, MW 296.36 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution, 3-((2-Fluorobenzyl)thio)-6-phenylpyridazine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 296.36 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), 3-((2-Fluorobenzyl)thio)-6-phenylpyridazine 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 FormulaC17H13FN2S
Molecular Weight296.36 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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.)1987
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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