7016-55-9

Basic information

• Product Name: BENZYLTRIETHYLPHOSPHONIUM BROMIDE
• Synonyms: BENZYLTRIETHYLPHOSPHONIUM BROMIDE
• CAS NO: 7016-55-9
• Molecular Formula: Br*C₁₃H₂₂P
• Molecular Weight: 289.19
• Mol File: 7016-55-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZYLTRIETHYLPHOSPHONIUM BROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYLTRIETHYLPHOSPHONIUM BROMIDE(7016-55-9)
• EPA Substance Registry System: BENZYLTRIETHYLPHOSPHONIUM BROMIDE(7016-55-9)

Safety Data

• Hazardous Substances Data: 7016-55-9(Hazardous Substances Data)

Upstream product

• 6588-00-7 ethyl diethylphosphinothioite 
• 100-39-0 benzyl bromide 
• 554-70-1 triethylphosphine 
• 100-51-6 benzyl alcohol 
• 121-44-8 triethylamine 

Downstream Products

• 51003-16-8 trans-1-(3,4-methylenedioxyphenyl)-2-phenylethylene 
• 83897-71-6 (Z)-1-Phenyl-1-tridecene 
• 42036-74-8 (E)-1-phenyltridec-1-ene 
• 117780-29-7 (E)-β-(1-decyl)styrene 
• 1657-49-4 1-chloro-4-[(Z)-2-phenylethenyl]benzene 
• 1657-50-7 (E)-1-(4-chlorophenyl)-2-phenylethene 
• 1694-20-8 trans-4-nitrostilbene 
• 6624-53-9 (Z)-1-nitro-4-(2-phenylethenyl)-benzene 
• 74809-43-1 trans-3,4,5-trimethoxystilbene 
• 645-49-8 cis-stilben 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 1694-19-5 E-1-(phenyl)-2-(4'-methoxyphenyl)ethene 
• 3892-92-0 (E)-3,4-dimethoxystilbene 
• 7642-18-4 (Z)-pent-1-en-1-ylbenzene 

Relevant articles and documents

Inhibition and Dispersion of Bacterial Biofilms with 2-Aminobenzimidazole Derivatives

Compounds described herein inhibit biofilm formation or disperse pre-formed biofilms of Gram-negative bacteria. Biofilm-inhibitory compounds can be encapsulated or contained in a polymer matrix for controlled release. Coatings, films, multilayer films, hydrogels, microspheres and nanospheres as well as pharmaceutical compositions and disinfecting compositions containing biofilm-inhibitory compounds are also provided. Methods for inhibiting formation of biofilms or dispersing already formed biofilms are provided. Methods for treating infections of gram-negative bacteria which form biofilms, particularly those of Pseudomonas and more particularly P. aeruginosa.

An iterative approach toward the synthesis of discrete oligomeric p-phenylene vinylene organic dyes employing aqueous Wittig chemistry

Photovoltaic research has become increasingly prominent as the search for alternatives to fossil fuels are actively sought. A novel process for the iterative synthesis of discrete donor/acceptor-flanked oligostilbenes, key constituents in dye-sensitized solar cells, is described. The aqueous Wittig process is high yielding, proceeds with high (E)-stereoselectivity and allows facile product purification.

GEMINAL SYSTEMS. 19. REACTIONS OF AMINOMETHYLPHOSPHINES WITH ELECTROPHILIC REAGENTS

-