99899-09-9

Basic information

• Product Name: Phenol, 2-[1-[[2-[(2-hydroxyethyl)amino]ethyl]imino]ethyl]-
• CAS NO: 99899-09-9
• Molecular Formula: C12H18N2O2
• Molecular Weight: 222.287
• Mol File: 99899-09-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[1-[[2-[(2-hydroxyethyl)amino]ethyl]imino]ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[1-[[2-[(2-hydroxyethyl)amino]ethyl]imino]ethyl]-(99899-09-9)
• EPA Substance Registry System: Phenol, 2-[1-[[2-[(2-hydroxyethyl)amino]ethyl]imino]ethyl]-(99899-09-9)

Safety Data

• Hazardous Substances Data: 99899-09-9(Hazardous Substances Data)

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 111-41-1 2-(2-Aminoethylamino)ethanol 

Downstream Products

• 744233-06-5 bis[μ-[2-[[[3-(5-hydroxy-κO)aza]pentyl]imine-κN]ethylphenolate(2-)-κO]]diboron 

Relevant articles and documents

Synthesis and characterization of dimeric μ-oxidovanadium complexes as the functional model of vanadium bromoperoxidase

Two vanadium (IV) complexes [VIVO(Haeae-sal)(MeOH)]+ (1) and [VIVO(Haeae-hyap)(MeOH)]+ (2) were prepared by reacting [VO(acac)2] with ligands [H2aeae-sal] (I) and [H2aeae-hyap] (II) respectively. Condensation of 2-(2-aminoethylamino)ethanol with salicylaldehyde and 2-hydroxyacetophenone produces the ligands (I) and (II) respectively. Both vanadium complexes 1 and 2 are sensitive towards aerial oxygen in solution and rapidly convert into vanadium(V) dioxido species. Vanadium(V) dioxido species crystalizes as the dimeric form in the solid-state. Single-crystal XRD analysis suggests octahedral geometry around each vanadium center in the solid-state. To access the benefits of heterogeneous catalysis, vanadium(V) dioxido complexes were anchored into the polymeric chain of chloromethylated polystyrene. All the synthesized neat and supported vanadium complexes have been studied by a number of techniques to confirm their structural and functional properties. Bromoperoxidase activity of the synthesized vanadium(V) dioxido complexes 3 and 4 was examined by carrying out oxidative bromination of salicylaldehyde and oxidation of thioanisole. In the presence of hydrogen peroxide, 3 shows 94.4% conversion (TOF value of 2.739 × 102 h?1) and 4 exhibits 79.0% conversion (TOF value of 2.403 × 102 h?1) for the oxidative bromination of salicylaldehyde where 5-bromosalicylaldehyde appears as the major product. Catalysts 3 and 4 also efficiently catalyze the oxidation of thioanisole in the presence of hydrogen peroxide where sulfoxide is observed as the major product. Covalent attachment of neat catalysts 3 and 4 into the polymer chain enhances substrate conversion (%) and their catalytic efficiency increases many folds, both in the oxidative bromination and oxidation of thioether. Polymer supported catalysts 5 displayed 98.8% conversion with a TOF value of 1.127 × 104 h?1 whereas catalyst 6 showed 95.7% conversion with a TOF value of 4.675 × 103 h?1 for the oxidative bromination of salicylaldehyde. These TOF values are the highest among the supported vanadium catalysts available in the literature for the oxidative bromination of salicylaldehyde.

Synthesis, structures, and antimicrobial activities of dimeric oxovanadium(V) complexes with tridentate schiff bases

Two new dimeric oxovanadium(V) complexes, [VO2L 1]2 (1) and [VO2L2]2 (2), where L1 and L2 are the monoanionic form of 2-{1-[2-(2-hydroxyethylamino)ethylimino]ethyl}phe