3-(2,6-Difluorophenyl)-4-[(piperidin-1-yl)methyl]-2,3-dihydro-1,3-thiazole-2-thione CAS 866153-88-0

Purity 97%+In StockPharmaceutical Standards
CAS No.866153-88-0
Molecular FormulaC15H16F2N2S2
Molecular Weight326.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2,6-Difluorophenyl)-4-[(piperidin-1-yl)methyl]-2,3-dihydro-1,3-thiazole-2-thione CAS 866153-88-0 chemical structure

Description

3-(2,6-Difluorophenyl)-4-[(piperidin-1-yl)methyl]-2,3-dihydro-1,3-thiazole-2-thione (C15H16F2N2S2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

3-(2,6-Difluorophenyl)-4-[(piperidin-1-yl)methyl]-2,3-dihydro-1,3-thiazole-2-thione (CAS 866153-88-0) is a high-purity analytical reference standard with the molecular formula C15H16F2N2S2 and a molecular weight of 326.43 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), 3-(2,6-Difluorophenyl)-4-[(piperidin-1-yl)methyl]-2,3-dihydro-1,3-thiazole-2-thione 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 FormulaC15H16F2N2S2
Molecular Weight326.43 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms2

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