6-(4-Fluorophenyl)-2-((3,4,4-trifluorobut-3-en-1-yl)thio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine CAS 343374-77-6

Purity 97%+In StockPharmaceutical Standards
CAS No.343374-77-6
Molecular FormulaC15H11F4N5S
Molecular Weight369.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(4-Fluorophenyl)-2-((3,4,4-trifluorobut-3-en-1-yl)thio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine CAS 343374-77-6 chemical structure

Description

6-(4-Fluorophenyl)-2-((3,4,4-trifluorobut-3-en-1-yl)thio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (C15H11F4N5S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution. Halogen substitution raises its density and boiling point; 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.

6-(4-Fluorophenyl)-2-((3,4,4-trifluorobut-3-en-1-yl)thio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CAS 343374-77-6) is a high-purity analytical reference standard with the molecular formula C15H11F4N5S and a molecular weight of 369.34 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.

CATO manufactures 6-(4-Fluorophenyl)-2-((3,4,4-trifluorobut-3-en-1-yl)thio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H11F4N5S
Molecular Weight369.34 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms5
Sulfur Atoms1

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