10319-02-5

Basic information

• Product Name: bis-(3-chloro-salicylidene)-ethylenediamine
• Synonyms: bis-(3-chloro-salicylidene)-ethylenediamine
• CAS NO: 10319-02-5
• Molecular Weight: 337.205
• Mol File: 10319-02-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: bis-(3-chloro-salicylidene)-ethylenediamine(CAS DataBase Reference)
• NIST Chemistry Reference: bis-(3-chloro-salicylidene)-ethylenediamine(10319-02-5)
• EPA Substance Registry System: bis-(3-chloro-salicylidene)-ethylenediamine(10319-02-5)

Safety Data

• Hazardous Substances Data: 10319-02-5(Hazardous Substances Data)

Upstream product

• 1927-94-2 3-chlorosalicylaldehyde 
• 107-15-3 ethylenediamine 

Downstream Products

• 1336921-71-1 (ClC₆H₃(OH))CH₂NHCH₂CH₂NHCH₂(C₆H₃(OH)Cl) 

Relevant articles and documents

Electrochemical properties of VO salen complexes

Electrochemical properties of a series of differently substituted vanadyl salen complexes were investigated using cyclic voltammetry in different solvents. Results obtained show that the salen structure stabilizes the oxidized forms and that the effects of substituents on the oxidation potential correlate with the electronic density of the metal. Also the role of the donicity of the solvent in influencing the redox potentials of the studied complexes has been evidenced. Moreover, the variations of the observed potentials can be qualitatively correlated to the catalytic activity of vanadyl salen derivatives in the oxidation of thioethers.

Major impact of N-methylation on cytotoxicity and hydrolysis of salan Ti(IV) complexes: Sterics and electronics are intertwined

A series of Ti(IV) complexes containing diamino bis(phenolato) "salan" type ligands with NH coordination were prepared, and their hydrolysis and cytotoxicity were analyzed and compared to the N-methylated analogues. Substituting methyl groups on the coord