5,7-Dimethyl-3-(thiophen-2-yl)-6-(3-(trifluoromethyl)benzyl)pyrazolo[1,5-a]pyrimidine CAS 900014-82-6

Purity 97%+In StockPharmaceutical Standards
CAS No.900014-82-6
Molecular FormulaC20H16F3N3S
Molecular Weight387.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5,7-Dimethyl-3-(thiophen-2-yl)-6-(3-(trifluoromethyl)benzyl)pyrazolo[1,5-a]pyrimidine CAS 900014-82-6 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution, 5,7-Dimethyl-3-(thiophen-2-yl)-6-(3-(trifluoromethyl)benzyl)pyrazolo[1,5-a]pyrimidine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 387.42 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

5,7-Dimethyl-3-(thiophen-2-yl)-6-(3-(trifluoromethyl)benzyl)pyrazolo[1,5-a]pyrimidine (CAS 900014-82-6) is a high-purity analytical reference standard with the molecular formula C20H16F3N3S and a molecular weight of 387.42 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), 5,7-Dimethyl-3-(thiophen-2-yl)-6-(3-(trifluoromethyl)benzyl)pyrazolo[1,5-a]pyrimidine 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 FormulaC20H16F3N3S
Molecular Weight387.42 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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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