CAS 120-70-7 N,N'-Bis(salicylidene)-1,3-propanediamine

Synonyms

J-004383; o-Cresol,.alpha.'-(trimethylenedinitrilo)di-; Disalicylidene propandiamine; AC1NUYZK; SCHEMBL710369; 133345-53-6; 6-[[3-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]propylamino]methylidene]cyclohexa-2,4-dien-1-one; AC1NSZDU; DTXSID7059513; NSC 166332;

IUPAC Name

2-[3-[(2-hydroxyphenyl)methylideneamino]propyliminomethyl]phenol;

Molecular Weight

282.343g/mol

Molecular Formula

C17H18N2O2;

Canonical SMILES

C1=CC=C(C(=C1)C=NCCCN=CC2=CC=CC=C2O)O;

InChI

InChI=1S/C17H18N2O2/c20-16-8-3-1-6-14(16)12-18-10-5-11-19-13-15-7-2-4-9-17(15)21/h1-4,6-9,12-13,20-21H,5,10-11H2;

InChI Key

KLDZYURQCUYZBL-UHFFFAOYSA-N;

Complexity

312

Covalently-Bonded Unit Count

EC Number

204-418-6

Exact Mass

282.137g/mol

H-Bond Acceptor

H-Bond Donor

Heavy Atom Count

Monoisotopic Mass

282.137g/mol

NSC Number

166332

Rotatable Bond Count

Topological Polar Surface Area

65.2A^2

Application

N,N'-Bis(salicylidene)-1,3-propanediamine is a versatile di-Schiff base ligand, utilized in the synthesis of various metal complexes and advanced materials. This compound, appearing as a light yellow to green powder or crystal, plays a crucial role in forming new trinuclear heterometallic Cu(II)-Mn(II) complexes and mononuclear nickel complexes. Additionally, it serves as a foundation for the preparation of an Al3+ ion-selective electrode, essential for quantifying trace amounts of aluminum. Its functionalization, involving sodium thioglycolate, enables the creation of Cu-ICP nanoparticles, showcasing its potential in diverse chemical applications.

March 5, 2025

Excellent Product for Complex Synthesis and Research Applications

N,N'-Bis(salicylidene)-1,3-propanediamine from Alfa Chemistry is ideal for synthesizing Cu(II)-Mn(II) complexes and nickel complex NiL in research. Effective as a base in ion-selective electrodes for trace Al detection.