195209-24-6

Basic information

• Product Name: 1-bromo-3,5-bis(diethoxyphosphorylmethyl)benzene
• Synonyms: 1-bromo-3,5-bis(diethoxyphosphorylmethyl)benzene
• CAS NO: 195209-24-6
• Molecular Weight: 457.238
• Mol File: 195209-24-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-bromo-3,5-bis(diethoxyphosphorylmethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-3,5-bis(diethoxyphosphorylmethyl)benzene(195209-24-6)
• EPA Substance Registry System: 1-bromo-3,5-bis(diethoxyphosphorylmethyl)benzene(195209-24-6)

Safety Data

• Hazardous Substances Data: 195209-24-6(Hazardous Substances Data)

Upstream product

• 51760-23-7 1-bromo-3,5-bis(bromomethyl)benzene 
• 51719-69-8 1-bromo-3-(bromomethyl)-5-methylbenzene 
• 122-52-1 triethyl phosphite 
• 556-96-7 5-bromo-1,3-xylene 

Downstream Products

• 240140-74-3 3,5-Bis-((E)-2-{3,5-bis-[(E)-2-(3,5-di-tert-butyl-phenyl)-vinyl]-phenyl}-vinyl)-benzaldehyde 
• 869959-67-1 C₄₁H₄₂N₂O₁₀ 
• 869959-66-0 3',5'-bis-[2-(2,4-dimethoxy-6-methoxycarbonyl-phenyl)-vinyl]-biphenyl-4-carboxylic acid 
• 869959-65-9 C₃₀H₂₉BrO₈ 
• 869959-64-8 C₂₈H₂₅BrO₈ 
• 363622-57-5 5-bromo-1,3-bis(p-cyanostyryl)benzene 
• 363622-55-3 1-bromo-3,5-bis(p-methoxystyryl)benzene 
• 240140-77-6 1-bromo-3,5-bis(3',5'-di-t-butylstyryl)benzene 

Relevant articles and documents

Synthesis of stilbene carboxylic acids as scaffolds for calcium sensors

This communication describes the synthesis and characterization of calcium binding stilbene carboxylic acids. The Royal Society of Chemistry 2005.

Synthetic bacteriochlorins bearing polar motifs (carboxylate, phosphonate, ammonium and a short PEG). Water-solubilization, bioconjugation, and photophysical properties

Bacteriochlorins are potentially excellent chromophores for near-infrared (NIR) photochemical and spectroscopic studies yet the intrinsically hydrophobic macrocycle core has stymied work in aqueous media. Herein, a set of bacteriochlorins bearing distinct

Synthesis, characterization, and optical response of dipolar and non-dipolar poly(phenylenevinylene) dendrimers

New dipolar and non-dipolar poly(phenylenevinylene) dendrimers bearing electron-donating and electron-withdrawing groups have been efficiently synthesized using Heck and Horner-Wadsworth-Emmons reactions. The photoluminescence of these systems may be tuned in the blue zone by choosing the appropriate peripheral groups. Despite the meta-substitution pattern, large Stokes shifts can be observed when π-donor and π-acceptor groups are connected by a m-phenylenevinylene system.