4-{naphtho[2,1-b]furan-2-yl}-2-(1H-pyrrol-1-yl)pyrimidine CAS 866131-74-0

Purity 97%+In StockPharmaceutical Standards
CAS No.866131-74-0
Molecular FormulaC20H13N3O
Molecular Weight311.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-{naphtho[2,1-b]furan-2-yl}-2-(1H-pyrrol-1-yl)pyrimidine CAS 866131-74-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 311.34 g/mol gives 4-{naphtho[2,1-b]furan-2-yl}-2-(1H-pyrrol-1-yl)pyrimidine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-{naphtho[2,1-b]furan-2-yl}-2-(1H-pyrrol-1-yl)pyrimidine (CAS 866131-74-0) is a high-purity analytical reference standard with the molecular formula C20H13N3O and a molecular weight of 311.34 g/mol.

4-{naphtho[2,1-b]furan-2-yl}-2-(1H-pyrrol-1-yl)pyrimidine (C20H13N3O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

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 FormulaC20H13N3O
Molecular Weight311.34 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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