2-Amino-3-(4-bromobenzoyl)-N-phenylindolizine-1-carboxamide CAS 896172-79-5

Purity 97%+In StockPharmaceutical Standards
CAS No.896172-79-5
Molecular FormulaC22H16BrN3O2
Molecular Weight434.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Amino-3-(4-bromobenzoyl)-N-phenylindolizine-1-carboxamide CAS 896172-79-5 chemical structure

Description

As a certified reference material (CRM), 2-Amino-3-(4-bromobenzoyl)-N-phenylindolizine-1-carboxamide 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.

2-Amino-3-(4-bromobenzoyl)-N-phenylindolizine-1-carboxamide (CAS 896172-79-5) is a high-purity analytical reference standard with the molecular formula C22H16BrN3O2 and a molecular weight of 434.29 g/mol.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution, 2-Amino-3-(4-bromobenzoyl)-N-phenylindolizine-1-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 434.29 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

Physical & Chemical Properties

Molecular FormulaC22H16BrN3O2
Molecular Weight434.29 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore in a cool place (≤25°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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentBr-containing
Nitrogen Atoms3

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