1-(3-Chlorophenyl)-3-phenyl-1,4-dihydrochromeno[4,3-b]pyrrole CAS 654651-12-4

Purity 97%+In StockPharmaceutical Standards
CAS No.654651-12-4
Molecular FormulaC23H16ClNO
Molecular Weight357.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Chlorophenyl)-3-phenyl-1,4-dihydrochromeno[4,3-b]pyrrole CAS 654651-12-4 chemical structure

Description

Structurally, 1-(3-Chlorophenyl)-3-phenyl-1,4-dihydrochromeno[4,3-b]pyrrole (C23H16ClNO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 16.0, corresponding to approximately 16 ring(s) or double-bond equivalent(s). With a molecular weight of 357.83 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

1-(3-Chlorophenyl)-3-phenyl-1,4-dihydrochromeno[4,3-b]pyrrole (CAS 654651-12-4) is a high-purity analytical reference standard with the molecular formula C23H16ClNO and a molecular weight of 357.83 g/mol.

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.

As a certified reference material (CRM), 1-(3-Chlorophenyl)-3-phenyl-1,4-dihydrochromeno[4,3-b]pyrrole 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 FormulaC23H16ClNO
Molecular Weight357.83 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms1

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