92194-03-1

Basic information

• Product Name: 4-BROMO-4'-DIMETHYLAMINOBIPHENYL
• Synonyms: 4-BROMO-4'-DIMETHYLAMINOBIPHENYL
• CAS NO: 92194-03-1
• Molecular Formula: C₁₄H₁₄BrN
• Molecular Weight: 276.17
• Mol File: 92194-03-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-BROMO-4'-DIMETHYLAMINOBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-4'-DIMETHYLAMINOBIPHENYL(92194-03-1)
• EPA Substance Registry System: 4-BROMO-4'-DIMETHYLAMINOBIPHENYL(92194-03-1)

Safety Data

• Hazardous Substances Data: 92194-03-1(Hazardous Substances Data)

Upstream product

• 92-86-4 4-(4-bromophenyl)bromobenzene 
• 506-59-2 N,N-dimethylammonium chloride 
• 93296-10-7 (4-(dimethylamino)phenyl)zinc(II) chloride 
• 106-53-6 para-bromobenzenethiol 
• 589-87-7 1,4-bromoiodobenzene 
• 28611-39-4 4-(dimethylamino)benzene-boronic acid 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 67-56-1 methanol 
• 3365-82-0 4-amino-4'-bromobiphenyl 
• 171364-78-6 (4-(N,N-dimethylamino)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 1190375-94-0 2-(4'-N,N-dimethylamino-1,1'-biphenyl-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 160035-91-6 tetra(4'-dimethylaminobiphenyl-4-yl)tin 

Relevant articles and documents

COMPOUNDS FOR USING IN IMAGING AND PARTICULARLY FOR THE DIAGNOSIS OF NEURODEGENERATIVE DISEASES

The invention relates to compounds of formula (II) for using in imaging and particularly for the diagnosis of neurodegenerative diseases

Fluorescent chemosensors of carbohydrate triols exhibiting TICT emissions

4-4′-Disubstituted biphenyl boronic acids (BBAs) are push-pull fluorophores with "turn-on" fluorescence properties. Upon carbohydrate triol binding, BBA boronate esters can participate in photon-induced electron transfer, giving a twisted intramolecular charge transfer (TICT) complex. The resulting TICT emissions distinguish between carbohydrates that bind to boron as a diol versus triol unit, thereby revealing stereochemical information about the carbohydrate.

Convenient methods for preparing ?-conjugated linkers as building blocks for modular chemistry

Simple, straightforward and optimized procedures for preparing extended ?-conjugated linkers are described. Either unsubstituted or 4-donor substituted ?-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl ?-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki-Miyaura or Sonogashira coupling reactions.