14467-68-6

Basic information

• Product Name: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[4-nitro-
• CAS NO: 14467-68-6
• Molecular Formula: C16H16N2O6
• Molecular Weight: 332.313
• Mol File: 14467-68-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[4-nitro-(14467-68-6)
• EPA Substance Registry System: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[4-nitro-(14467-68-6)

Safety Data

• Hazardous Substances Data: 14467-68-6(Hazardous Substances Data)

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 1124-31-8 potassium 4-nitrophenolate 
• 100-02-7 4-nitro-phenol 
• 6940-78-9 4-chlorobutyl bromide 
• 824-78-2 4-nitrophenol sodium salt 
• 628-21-7 1,4-Diiodobutane 
• 110-63-4 Butane-1,4-diol 
• 100-00-5 4-chlorobenzonitrile 

Downstream Products

• 127227-57-0 1-<4-(hydroxymethyl)phenoxy>-4-1-(N⁴-phenlylpiperazinyl)>butane 
• 146885-99-6 1,3-di(dithiourea-4-phenoxy)-butane 
• 127227-55-8 4-[4-(4-Phenyl-piperazin-1-yl)-butoxy]-benzaldehyde 
• 104209-31-6 1,4-bis(4-acetamidophenoxy)butane 
• 6245-50-7 4-[4-(4-aminophenoxy)butoxy]aniline 

Relevant articles and documents

BIVALENT LECA INHIBITORS TARGETING BIOFILM FORMATION OF PSEUDOMONAS AERUGINOSA

The present invention relates to divalent compounds binding to LecA. The compounds are useful to block biofilm formation of Pseudomonas aeruginosa. The invention further relates to pharmaceutical compositions comprising these compounds and to therapeutic methods and uses of these compounds, in particular to therapeutic methods and uses for the treatment of Pseudomonas aeruginosa infections in a subject. The invention also relates to imaging of infections, such as biofilms produced by Pseudomonas aeruginosa, by using these divalent compounds.

Facile one-pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers under mild conditions

We report here the facile, room temperature, catalyst free, one pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers. Anhydrous potassium carbonate (K2CO3) as a mild base along with dimethyl sulfoxide gener

Biological properties of amidinium sulfinic and sulfonic acid derivatives: inhibition of glycolytic enzymes of Trypanosoma brucei and protective effect on cell growth

The activity of the title compounds has been investigated on two biological targets: cultures of trypanosome and glycolytic enzymes inhibition of the parasite, and on retinal epithelium cells.In both cases, these compounds exhibit a significant activity,