3-(4-Fluorophenyl)-6-(2-methylpropane-2-sulfonyl)pyrazolo[1,5-a]pyrimidin-7-amine CAS 865658-03-3

Purity 97%+In StockPharmaceutical Standards
CAS No.865658-03-3
Molecular FormulaC16H17FN4O2S
Molecular Weight348.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Fluorophenyl)-6-(2-methylpropane-2-sulfonyl)pyrazolo[1,5-a]pyrimidin-7-amine CAS 865658-03-3 chemical structure

Description

CATO manufactures 3-(4-Fluorophenyl)-6-(2-methylpropane-2-sulfonyl)pyrazolo[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.

3-(4-Fluorophenyl)-6-(2-methylpropane-2-sulfonyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS 865658-03-3), molecular formula C16H17FN4O2S and molecular weight 348.40 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, 3-(4-Fluorophenyl)-6-(2-methylpropane-2-sulfonyl)pyrazolo[1,5-a]pyrimidin-7-amine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 348.40 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC16H17FN4O2S
Molecular Weight348.40 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms4
Sulfur Atoms1

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