N-(3-Phenylallylidene)-9H-fluoren-2-amine CAS 5439-53-2

Purity 97%+In StockPharmaceutical Standards
CAS No.5439-53-2
Molecular FormulaC22H17N
Molecular Weight295.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Phenylallylidene)-9H-fluoren-2-amine CAS 5439-53-2 chemical structure

Description

The occurrence of N-(3-Phenylallylidene)-9H-fluoren-2-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 N-(3-Phenylallylidene)-9H-fluoren-2-amine (CAS 5439-53-2), a certified reference material (molecular formula C22H17N, MW 295.38 g/mol) for analytical method development and quality control.

The molecular framework of N-(3-Phenylallylidene)-9H-fluoren-2-amine (C22H17N) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

CATO manufactures N-(3-Phenylallylidene)-9H-fluoren-2-amine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC22H17N
Molecular Weight295.38 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms1

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