4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one CAS 62460-53-1

Purity 97%+In StockPharmaceutical Standards
CAS No.62460-53-1
Molecular FormulaC13H10N4O
Molecular Weight238.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one CAS 62460-53-1 chemical structure

Description

The occurrence of 4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one (CAS 62460-53-1), molecular formula C13H10N4O and molecular weight 238.24 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 238.24 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).

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), 4-Phenyl-6-(1H-pyrrol-2-yl)-1,3,5-triazin-2(1H)-one 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 FormulaC13H10N4O
Molecular Weight238.24 g/mol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Nitrogen Atoms4

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