4044-95-5

Basic information

• Product Name: 3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE
• Synonyms: BUTTPARK 89\03-26;3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE
• CAS NO: 4044-95-5
• Molecular Formula: C₁₃H₉BrN₂
• Molecular Weight: 273.13
• Mol File: 4044-95-5.mol
• Article Data: 24

Chemical Properties

• Melting Point: 88-90 °C
• Appearance: /
• Density: 1.48 g/cm³
• Refractive Index: 1.676
• PKA: 3.73±0.50(Predicted)
• CAS DataBase Reference: 3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE(4044-95-5)
• EPA Substance Registry System: 3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE(4044-95-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 4044-95-5(Hazardous Substances Data)

Usage

General Description

3-Bromo-2-phenyl-imidazo[1,2-a]pyridine is a chemical compound with the molecular formula C13H9BrN2. It is a derivative of imidazo[1,2-a]pyridine, a heterocyclic compound. 3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIDINE contains a phenyl group and a bromine atom attached to the imidazo[1,2-a]pyridine ring structure. It has potential applications in medicinal chemistry and drug development, as imidazo[1,2-a]pyridine derivatives have been studied for their pharmacological activities, including anticancer, antimicrobial, and antiviral properties. The specific properties and uses of 3-bromo-2-phenyl-imidazo[1,2-a]pyridine may vary based on further research and development in the field of organic chemistry and pharmaceutical sciences.

InChI:InChI=1/C13H9BrN2/c14-13-12(10-6-2-1-3-7-10)15-11-8-4-5-9-16(11)13/h1-9H

Upstream product

• 3672-37-5 3-nitroso-2-phenylimidazo<1,2-a>pyridine 
• 4105-21-9 2-phenylimidazo[1,2-a]pyridine 
• 1883-96-1 N-benzylidenepyridin-2-amine 
• 75-25-2 Bromoform 
• 1373338-15-8 2-iodoimidazo[1,2-a]pyridine 
• 98-80-6 phenylboronic acid 
• 504-29-0 2-aminopyridine 
• 70-11-1 α-bromoacetophenone 
• 3672-39-7 2-phenylimidazo[1,2-a]pyridine-3-carbaldehyde 
• 3323-66-8 2-phenyl-imidazo[1,2-a]pyridine; hydrobromide 
• 98-86-2 acetophenone 
• 57957-24-1 N-(1-phenylvinyl)acetamide 
• 110-86-1 pyridine 
• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 

Downstream Products

• 1353511-55-3 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine 
• 85102-26-7 2,3-diphenyl-1H-imidazo[1,2-a]pyridine 
• 34658-68-9 3-methyl-2-phenyl-1H-imidazo[1,2-a]pyridine 
• 1416319-49-7 2-phenyl-3-(p-tolyl)imidazo[1,2-a]pyridine 
• 1416319-50-0 3-(4-methoxyphenyl)-2-phenylimidazo[1,2-a]pyridine 
• 4105-21-9 2-phenylimidazo[1,2-a]pyridine 
• 1116088-85-7 methyl (E)-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)acrylate 
• 869583-82-4 2-phenyl-3-(2-phenylethynyl)imidazo[1,2-a]pyridine 
• 22244-94-6 3-nitro-2-(4'-nitrophenyl)imidazo[1,2-a]pyridine 
• 22244-95-7 3-bromo-2-(4'-nitrophenyl)imidazo[1,2-a]pyridine 

Relevant articles and documents

Oxidative C-H/C-H Annulation of Imidazopyridines and Indazoles through Rhodium-Catalyzed Vinylene Transfer

Transition-metal-catalyzed C-H activation followed by oxidative annulation with alkynes has been an efficient synthetic tool for the assembly of various polyaromatic scaffolds. Despite the substantial progress in this field, it is still a significant chal

Metal-free oxidative decarbonylative halogenation of fused imidazoles

An efficient strategy has been developed for the deformylative halogenation of carbaldehyde imidazo-fused heterocycles in the presence of TBHP controlled by temperature. A convenient and sequential functionalization (C8 to C3) portrays the synthetic utility of the current method.N-Heterocycle benzamide products were also observedviathe ring opening of imidazopyridines through the cleavage of C-C bond at high temperatures. Features of this method include temperature-controlled excellent regioselectivity, mild conditions and functional group tolerance.

Preparation method of C-3 haloimidazolium [1,2-a] pyridine derivative

The present invention discloses a method for preparing a C-3 haloimidazolium [1,2-a] pyridine derivative, belonging to the field of organic synthesis. The method took imidazolium [1,2-a] pyridine as the starting material, halide cuprous as the halogen sou