3-(4-Chlorophenyl)-6-tosylpyrazolo[1,5-a]pyrimidin-7-amine CAS 439109-02-1

Purity 97%+In StockPharmaceutical Standards
CAS No.439109-02-1
Molecular FormulaC19H15ClN4O2S
Molecular Weight398.87 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Chlorophenyl)-6-tosylpyrazolo[1,5-a]pyrimidin-7-amine CAS 439109-02-1 chemical structure

Description

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.

3-(4-Chlorophenyl)-6-tosylpyrazolo[1,5-a]pyrimidin-7-amine (CAS 439109-02-1), molecular formula C19H15ClN4O2S and molecular weight 398.87 g/mol, is a CATO reference standard with documented purity and traceability.

3-(4-Chlorophenyl)-6-tosylpyrazolo[1,5-a]pyrimidin-7-amine (C19H15ClN4O2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, 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).

CATO manufactures 3-(4-Chlorophenyl)-6-tosylpyrazolo[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 FormulaC19H15ClN4O2S
Molecular Weight398.87 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms1

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