125808-05-1

Basic information

• Product Name: 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene
• Synonyms: 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene
• CAS NO: 125808-05-1
• Molecular Weight: 319.195
• Mol File: 125808-05-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene(125808-05-1)
• EPA Substance Registry System: 1-bromo-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene(125808-05-1)

Safety Data

• Hazardous Substances Data: 125808-05-1(Hazardous Substances Data)

Upstream product

• 106-41-2 4-bromo-phenol 
• 62921-74-8 2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate 
• 112-35-6 triethylene glucol monomethyl ether 
• 123824-56-6 1-bromo-6-phenyl-3,6-dioxahexane 
• 7204-16-2 2-(2-(2-phenoxyethoxy)ethoxy)ethan-1-ol 
• 104-68-7 2-(2-phenoxyethoxy)ethanol 
• 80392-33-2 1-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)benzene 
• 123824-57-7 1-bromo-9-phenyl-3,6,9-trioxanonane 

Downstream Products

• 1337529-95-9 C₅₉H₈₆N₁₁O₁₈P 
• 1337529-85-7 dimethyl-4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphonite 
• 1078714-74-5 [2-(4-(2-[2-(2-methoxyethoxy)ethoxy]ethoxy)phenyl)ethynyl]trimethylsilane 
• 1446448-43-6 1-iodo-4-((4-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenyl)ethynyl)benzene 

Relevant articles and documents

Live-cell one- And two-photon uncaging of a far-red emitting acridinone fluorophore

Total synthesis and photophysical properties of PENB-DDAO, a photoactivatable 1,3-dichloro9,9-dimethyl-9H-acrldln-2(7)-one (DDAO) derivative of a far-red emitting fluorophore, are described. The photoremovable group of the DDAO phenolic function comprises a donor/acceptor blphenyl platform which allows an efficient (>95%) and rapid (a.Φu = 3.7 GM at 740 nm). PENB-DDAO Is cell permeable as demonstrated by the triggering of cytoplasmic red fluorescent signal In HeLa cells after one-photon Irradiation (λexc around 360 nm) or by the generation of a red fluorescent signal In a delineated area of a single cell after two-photon photoactivation (λexc = 770 nm).

N,N,N',N'-TETRAPHENYL BENZIDINE COMPOUND

PROBLEM TO BE SOLVED: To provide an N,N,N',N'-tetraphenyl benzidine compound to be used as a source material of a polymer containing a fluorine atom suitable for a charge transporting varnish that gives a thin film, with which an organic EL element having excellent luminance characteristics can be achieved, even when the film is used as a single layer in a state of disposed between and in contact with an anode and a luminescent layer. SOLUTION: The N,N,N',N'-tetraphenyl benzidine compound is represented by formula (9-1). In the formula, Z2 represents an alkoxy group having 1 to 20 carbon atoms which may include an ether bone, however, Z2 as a methoxy group or n-octyloxy group substituted at a para-position of an amino group is excluded. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Staudinger-phosphonite reactions for the chemoselective transformation of azido-containing peptides and proteins

Site-specific functionalization of proteins by bioorthogonal modification offers a convenient pathway to create, modify, and study biologically active biopolymers. In this paper the Staudinger reaction of aryl-phosphonites for the chemoselective functiona