Atomfair N-(5-(phenylamino)penta-2,5-dienylidene)aniline monohydrochloride Glutacondianil hydrochloride C17H17ClN2

Description N-(5-(Phenylamino)penta-2,5-dienylidene)aniline monohydrochloride (CAS No. 1497-49-0) is a high-purity organic compound with the molecular formula C17H17ClN2. This hydrochloride salt derivative of glutacondianil is a valuable intermediate in synthetic organic chemistry, particularly in the preparation of dyes, pigments, and functional materials. Its conjugated diene structure and aromatic substituents make it a versatile building block for researchers exploring photochemical properties, polymerization, or ligand design. Available in >95% purity (HPLC), this compound is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency for research applications. Proper storage at 2-8??C under inert atmosphere is recommended for long-term stability.

Description

N-(5-(Phenylamino)penta-2,5-dienylidene)aniline monohydrochloride (CAS No. 1497-49-0) is a high-purity organic compound with the molecular formula C₁₇H₁₇ClN₂. This hydrochloride salt derivative of glutacondianil is a valuable intermediate in synthetic organic chemistry, particularly in the preparation of dyes, pigments, and functional materials. Its conjugated diene structure and aromatic substituents make it a versatile building block for researchers exploring photochemical properties, polymerization, or ligand design. Available in >95% purity (HPLC), this compound is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency for research applications. Proper storage at 2-8??C under inert atmosphere is recommended for long-term stability.

CAS No: 1497-49-0
Molecular Formula: C17H17ClN2
Molecular Weight: 284.8
Exact Mass: 284.1080262
Monoisotopic Mass: 284.1080262
IUPAC Name: N-(5-phenyliminopenta-1,3-dienyl)aniline;hydrochloride
SMILES: C1=CC=C(C=C1)NC=CC=CC=NC2=CC=CC=C2.Cl
Synonyms: N-(5-(Phenylamino)penta-2,5-dienylidene)aniline monohydrochloride, N-[5-(phenylamino)penta-2,5-dienylidene]aniline monohydrochloride, Glutacondianil hydrochloride, Glutaconaldehyde dianilide hydrochloride, Pentadienedianiline hydrochloride

Application

This compound serves as a key precursor in the synthesis of conjugated organic materials with potential optoelectronic applications. Researchers utilize it in the development of Schiff base ligands for coordination chemistry and catalysis. Its diene structure makes it valuable for Diels-Alder reactions in pharmaceutical intermediate synthesis. The hydrochloride form improves solubility for reactions in polar solvents while maintaining the reactivity of the dienyl-aniline framework.

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