6-(Trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine CAS 1780-78-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1780-78-5
Molecular FormulaC18H20BrClN6O16P4
Molecular Weight815.63 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(Trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine CAS 1780-78-5 chemical structure

Description

Owing to a flavonoid core, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, 6-(Trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 815.63 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.

6-(Trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (CAS 1780-78-5), molecular formula C18H20BrClN6O16P4 and molecular weight 815.63 g/mol, is a CATO reference standard with documented purity and traceability.

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.

CATO manufactures 6-(Trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-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 FormulaC18H20BrClN6O16P4
Molecular Weight815.63 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentCl/Br-containing
Nitrogen Atoms6

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