Ethyl 5-(1-naphthyl)-7-(trifluoromethyl)pyrazolo-[1,5-a]pyrimidine-3-carboxylate CAS 679830-65-0

Purity 97%+In StockPharmaceutical Standards
CAS No.679830-65-0
Molecular FormulaC20H14F3N3O2
Molecular Weight385.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-(1-naphthyl)-7-(trifluoromethyl)pyrazolo-[1,5-a]pyrimidine-3-carboxylate CAS 679830-65-0 chemical structure

Description

CATO supplies Ethyl 5-(1-naphthyl)-7-(trifluoromethyl)pyrazolo-[1,5-a]pyrimidine-3-carboxylate (CAS 679830-65-0), a certified reference material (molecular formula C20H14F3N3O2, MW 385.34 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, Ethyl 5-(1-naphthyl)-7-(trifluoromethyl)pyrazolo-[1,5-a]pyrimidine-3-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 385.34 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC20H14F3N3O2
Molecular Weight385.34 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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.)1985
Halogen ContentF-containing
Nitrogen Atoms3

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