3-(2,3-Dihydro-1h-inden-5-yl)-1-phenyl-1h-pyrazol-5-amine CAS 956411-52-2

Purity 97%+In StockPharmaceutical Standards
CAS No.956411-52-2
Molecular FormulaC18H17N3
Molecular Weight275.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2,3-Dihydro-1h-inden-5-yl)-1-phenyl-1h-pyrazol-5-amine CAS 956411-52-2 chemical structure

Description

The occurrence of 3-(2,3-Dihydro-1h-inden-5-yl)-1-phenyl-1h-pyrazol-5-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(2,3-Dihydro-1h-inden-5-yl)-1-phenyl-1h-pyrazol-5-amine (CAS 956411-52-2), a certified reference material (molecular formula C18H17N3, MW 275.35 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 3-(2,3-Dihydro-1h-inden-5-yl)-1-phenyl-1h-pyrazol-5-amine is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 275.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC18H17N3
Molecular Weight275.35 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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