7147-52-6

Usage

Uses

Used in Organic Synthesis:
N-(5-Bromobiphenyl-2-yl)acetamide is used as a building block for the synthesis of various biologically active molecules. Its unique structure allows for the creation of a wide range of organic compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(5-Bromobiphenyl-2-yl)acetamide is utilized as a precursor for the development of new pharmaceutical agents. Its potential pharmacological properties make it a promising candidate for therapeutic applications, which are currently under investigation.
Used as a Reagent in Chemical Reactions:
N-(5-Bromobiphenyl-2-yl)acetamide also serves as a reagent in various chemical reactions, facilitating the synthesis of complex organic compounds and contributing to the advancement of chemical research.
Used in the Manufacturing of Novel Organic Compounds:
As a precursor, N-(5-Bromobiphenyl-2-yl)acetamide is instrumental in the production of innovative organic compounds, expanding the scope of chemical possibilities and applications in multiple industries.

InChI:InChI=1/C14H12BrNO/c1-10(17)16-14-8-7-12(15)9-13(14)11-5-3-2-4-6-11/h2-9H,1H3,(H,16,17)

Upstream product

• 2113-47-5 2-acetamidobiphenyl 
• 64-17-5 ethanol 
• 106736-41-8 N-biphenyl-2-yl-N-bromo-acetamide 
• 64-19-7 acetic acid 
• 108-90-7 chlorobenzene 
• 76-03-9 trichloroacetic acid 
• 86-00-0 2-nitrobiphenyl 
• 103-88-8 4-bromoacetanilide 
• 98-80-6 phenylboronic acid 
• 90-41-5 2-phenylaniline 
• 860572-11-8 N-biphenyl-2-yl-N-chloro-acetamide 
• 7726-95-6 bromine 

Downstream Products

• 16372-96-6 3,5-dibromo-1,1′-biphenyl 
• 861081-31-4 N-(3,5-dibromo-biphenyl-2-yl)-benzamide 
• 7511-41-3 2-benzamido-5-bromobiphenyl 
• 19111-87-6 2-bromobenzo[9,10]phenanthrene 
• 27353-48-6 2-bromo-phenanthridin-6-ol 
• 16372-95-5 2.4-Dibrom-6-phenylanilin 
• 5455-13-0 2-amino-5-bromobiphenyl 

Relevant academic research and scientific papers

Ruthenium(II)-catalyzed C-H arylation of anilides with boronic acids, borinic acids and potassium trifluoroborates

An in situ generated cationic ruthen-ium(II) catalyst allowed for robust C-H arylations of anilides with boronic acids. The optimized ruthenium catalyst was found to be both site selective and chemoselective, thereby providing the monoarylated products in

Ruthenium-catalyzed ortho-arylation of acetanilides with aromatic boronic acids: An easy route to prepare phenanthridines and carbazoles

The highly regioselective ortho-arylation of acetanilides with aromatic boronic acids in the presence of a Ru(ii) complex (3 mol%), AgSbF6 (12 mol%), Cu(OTf)2 (20 mol%) and Ag2O (1.0 eq.) is described. Later, ortho-arylated acetanilides were converted into phenanthridine and carbazole derivatives by using Ph3PO and Tf2O or palladium or Cu(OTf)2 catalysts.

QUATERNARY AMMONIUM SALT COMPOUNDS

[Problem] The object of the present invention is to provide a novel compound having 132 adrenergic receptor agonist activity and muscarinic receptor antagonist activity. [Means for Solving the Problem] The present invention is a quaternary ammonium salt compounds represented by formula (I), or a pharmaceutically acceptable salt thereof, with superior β32 adrenergic receptor agonist activity and muscarinic receptor antagonist activity.