256387-75-4

Basic information

• Product Name: 4,4'-bis(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-3,3'-dimethoxybiphenyl
• Synonyms: 4,4'-bis(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-3,3'-dimethoxybiphenyl
• CAS NO: 256387-75-4
• Molecular Weight: 466.19
• Mol File: 256387-75-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4'-bis(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-3,3'-dimethoxybiphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-bis(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-3,3'-dimethoxybiphenyl(256387-75-4)
• EPA Substance Registry System: 4,4'-bis(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-3,3'-dimethoxybiphenyl(256387-75-4)

Safety Data

• Hazardous Substances Data: 256387-75-4(Hazardous Substances Data)

Upstream product

• 25240-59-9 pinacolboronic acid 
• 92160-61-7 4,4'-diiodo-3,3'-dimethoxylbiphenyl 
• 84633-94-3 o-dianisidine bisdiazotated zinc doublesalt 
• 91-91-8 fast blue B 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 256387-76-5 6⁴,1⁴-diiodo-6³,5²,4³,3²,2³,1³-hexamethoxy-p-sexiphenyl 
• 1032671-04-7 4,4'''''-diiodo-[1,4';1',1'';4'',4''';1''',1'''';4'''',1''''']sexiphenyl-3,2',2'',2''',2'''',3'''''-hexaol 
• 881846-30-6 1⁶,8⁶-dimethyl-1²,2²,3³,4²,5³,6²,7³,8²-octamethoxy-p-octiphenyl 

Relevant articles and documents

Interface engineering of synthetic pores: Towards hypersensitive biosensors

Hydrophilic anchoring is introduced as a promising strategy to constructively control the various interactions of synthetic pore sensors with the surrounding biphasic environment. Artificial rigid-rod β barrels are selected as classical synthetic multifun

Electrostatics of cell membrane recognition: Structure and activity of neutral and cationic rigid push-pull rods in isoelectric, anionic, and polarized lipid bilayer membranes

Design, synthesis, and structural and functional studies of rigid-rod ionophores of different axial electrostatic asymmetry are reported. The employed design strategy emphasized presence of (a) a rigid scaffold to minimize the conformational complexity, (b) a unimolecular ion-conducting pathway to minimize the suprastructural complexity and monitor the function, (c) an extended fluorophore to monitor structure, (d) variable axial rod dipole, and (e) variable terminal charges to create axial asymmetry. Studies in isoelectric, anionic, and polarized bilayer membranes confirmed a general increase in activity of uncharged rigid push-pull rods in polarized bilayers. The similarly increased activity of cationic rigid push-pull rods with an electrostatic asymmetry comparable to that of α-helical bee toxin melittin (positive charge near negative axial dipole terminus) is shown by fluorescence-depth quenching experiments to originate from the stabilization of transmembrane rod orientation by the membrane potential. The reduced activity of rigid push-pull rods having an electrostatic asymmetry comparable to that in α-helical natural antibiotics (a positive charge near the positive axial dipole terminus) is shown by structural studies to originate from rod "ejection" by membrane potentials comparable to that found in mammalian plasma membranes. This structural evidence for cell membrane recognition by asymmetric rods is unprecedented and of possible practical importance with regard to antibiotic resistance.