16434-79-0

Basic information

• Product Name: Phenol, 2,4-dibromo-6-[(phenylimino)methyl]-
• CAS NO: 16434-79-0
• Molecular Formula: C13H9Br2NO
• Molecular Weight: 355.029
• Mol File: 16434-79-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 2,4-dibromo-6-[(phenylimino)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,4-dibromo-6-[(phenylimino)methyl]-(16434-79-0)
• EPA Substance Registry System: Phenol, 2,4-dibromo-6-[(phenylimino)methyl]-(16434-79-0)

Safety Data

• Hazardous Substances Data: 16434-79-0(Hazardous Substances Data)

Upstream product

• 90-59-5 3,5-Dibromosalicylaldehyde 
• 62-53-3 aniline 
• 90-02-8 salicylaldehyde 
• 861340-41-2 2,4-dibromo-6-dibromomethyl-phenol 
• 861315-28-8 2,4-dibromo-6-dichloromethyl-phenol 

Downstream Products

• 448923-01-1 bis(3,5-dibromosalicylideneaniline)diaquocobalt(II) 
• 1039041-52-5 [C₆H₅N=CH(OC₆H₂Br₂-2,4)]VCl₂(THF)2 
• 448923-00-0 bis(3,5-dibromosalicylideneaniline)diaquomanganese(II) 
• 448923-04-4 bis(3,5-dibromosalicylideneaniline)diaquocadmium(II) 
• 448923-03-3 bis(3,5-dibromosalicylideneaniline)diaquocopper(II) 
• 448923-02-2 bis(3,5-dibromosalicylideneaniline)diaquonickel(II) 
• 152600-22-1 {Ru(P(C₆H₅)3)2(C₆H₂(Br)2(O)CHN(C₆H₅))2} 

Relevant articles and documents

Anion binding ability and cytotoxicity of a selective colorimetric chemosensor for H2S based on Zn(Ⅱ) complex

A zinc(II) complex–based selective colorimetric chemosensor for H2S was synthesized. The ligand and complex crystals were obtained, and the molecular structures were confirmed by single-crystal X-ray diffraction analysis in addition to electros

Halide substituted Schiff-bases: Different activities in methyltrioxorhenium(VII) catalyzed epoxidation via different substitution patterns

This report shows the influence of halide substituted Schiff-bases as ligands of methyltrioxorhenium (MTO) in epoxidation catalysis. Therefore, selected Schiff-bases were prepared by the reaction of hydroxy-benzaldehydes and aniline derivates. These differently substituted Schiff-bases were tested as MTO-ligands in cyclooctene-and 1-octene-epoxidation. Although no great disparities among the substitution patterns have been found, some conclusions can be drawn. Flourines are inferior to chlorines or bromines as substituents. Halides in ortho-position lead to higher activities than in para-or meta-position. The balance between electron donating and withdrawing influences at the Schiff-base plays a prominent role in their utility as ligand to MTO in epoxidation catalysis.