7147-52-6

Basic information

• Product Name: N-(5-Bromobiphenyl-2-yl)acetamide
• Synonyms: 4'-Bromo-2'-phenylacetanilide;N-(5-Bromobiphenyl-2-yl)acetamide;Acetamide,N-(5-bromo[1,1'-biphenyl]-2-yl)-
• CAS NO: 7147-52-6
• Molecular Formula: C₁₄H₁₂BrNO
• Molecular Weight: 290.15518
• Mol File: 7147-52-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 403.7°Cat760mmHg
• Flash Point: 197.9°C
• Appearance: /
• Density: 1.422g/cm³
• Vapor Pressure: 9.99E-07mmHg at 25°C
• Refractive Index: 1.632
• CAS DataBase Reference: N-(5-Bromobiphenyl-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5-Bromobiphenyl-2-yl)acetamide(7147-52-6)
• EPA Substance Registry System: N-(5-Bromobiphenyl-2-yl)acetamide(7147-52-6)

Safety Data

• Hazardous Substances Data: 7147-52-6(Hazardous Substances Data)

Usage

General Description

N-(5-Bromobiphenyl-2-yl)acetamide, also known as 2-Acetylamino-5-bromobiphenyl, is a chemical compound with the molecular formula C16H13BrNO. It is a derivative of biphenyl, containing a bromine atom and an acetamide functional group. N-(5-Bromobiphenyl-2-yl)acetamide is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active molecules and pharmaceutical agents. It is also utilized as a reagent in chemical reactions and as a precursor in the manufacturing of novel organic compounds. N-(5-Bromobiphenyl-2-yl)acetamide exhibits potential pharmacological properties and has been studied for its potential therapeutic applications. Its structure and properties make it a valuable tool in various chemical and pharmaceutical applications.

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

• 106736-41-8 N-biphenyl-2-yl-N-bromo-acetamide 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 
• 108-90-7 chlorobenzene 
• 76-03-9 trichloroacetic acid 
• 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 
• 86-00-0 2-nitrobiphenyl 
• 2113-47-5 2-acetamidobiphenyl 
• 7726-95-6 bromine 

Downstream Products

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

Relevant articles and documents

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

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.