162586-73-4

Basic information

• Product Name: Phenol, 2,2'-[1,2-ethanediylbis(iminomethylene)]bis[4-bromo-
• CAS NO: 162586-73-4
• Molecular Formula: C16H18Br2N2O2
• Molecular Weight: 430.139
• Mol File: 162586-73-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 2,2'-[1,2-ethanediylbis(iminomethylene)]bis[4-bromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,2'-[1,2-ethanediylbis(iminomethylene)]bis[4-bromo-(162586-73-4)
• EPA Substance Registry System: Phenol, 2,2'-[1,2-ethanediylbis(iminomethylene)]bis[4-bromo-(162586-73-4)

Safety Data

• Hazardous Substances Data: 162586-73-4(Hazardous Substances Data)

Upstream product

• 1761-61-1 5-bromosalicyclaldehyde 
• 17937-38-1 N,N'-bis(5-bromosalicylidene)ethane-1,2-diamine 

Downstream Products

• 1146689-32-8 N,N'-dimethyl-N,N'-bis[(5-bromo-2-hydroxyphenyl)methylene]-1,2-diaminoethane 

Relevant articles and documents

Synthesis and antibacterial studies of some reduced schiff base derivatives

A series of N,N-substituted ethylene-1,2-diamine derivatives have been prepared from reaction of 2-hydroxybenzaldehyde derivatives and 1,2-diamine derivatives in the presence of NaBH4 through Schiff base intermediate. The synthesized compounds were screened for their antibacterial activities. Compound SB01, SB02 and SB09 displayed significant activity at MIC ranges from 0.40-6.25 μg/mL.

Synthesis and antimicrobial activity of N,N′-bis(2-hydroxylbenzyl)-1, 2-ethanediamine derivatives

A series of N,N′-Bis(2-hydroxylbenzyl)-1,2-ethanediamine derivatives and its schiff bases were synthesized, characterized and screened for in vitro antimicrobial activity against Staphylococcus aureus, Pseudomonas aeruginosa and Salmonella enterica. Resul