4805-70-3

Basic information

• Product Name: 3-BROMO-2-METHYLIMIDAZO[1,2-A]PYRIDINE
• Synonyms: 3-BROMO-2-METHYLIMIDAZO[1,2-A]PYRIDINE
• CAS NO: 4805-70-3
• Molecular Formula: C₈H₇BrN₂
• Molecular Weight: 211.06
• Mol File: 4805-70-3.mol
• Article Data: 9

Chemical Properties

• Melting Point: 73 °C
• Boiling Point: 1.6 g/cm³
• Appearance: /
• Density: 1.60±0.1 g/cm3(Predicted)
• PKA: 6.05±0.10(Predicted)
• CAS DataBase Reference: 3-BROMO-2-METHYLIMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-2-METHYLIMIDAZO[1,2-A]PYRIDINE(4805-70-3)
• EPA Substance Registry System: 3-BROMO-2-METHYLIMIDAZO[1,2-A]PYRIDINE(4805-70-3)

Safety Data

• Hazardous Substances Data: 4805-70-3(Hazardous Substances Data)

Usage

General Description

3-Bromo-2-methylimidazo[1,2-a]pyridine, also known as C9H8BrN3, is a chemical compound that falls under the category of heterocyclic compounds. The main features of these organic compounds are they have at least one atom in the ring that is not a carbon atom, which in this case, includes atoms of bromine and nitrogen. This chemical is represented by a molecular weight of 230.089 g/mol. In structural terms, 3-Bromo-2-methylimidazo[1,2-a]pyridine consists of a pyridine ring fused with an imidazole ring. Its utility primarily lies in research and laboratory settings. However, detailed information about its specific uses, handling precautions, and safety guidelines may vary based on its application and should always be obtained from a reliable source.

Upstream product

• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 
• 1373338-15-8 2-iodoimidazo[1,2-a]pyridine 
• 13061-96-6 dihydroxy-methyl-borane 
• 504-29-0 2-aminopyridine 
• 598-31-2 1-bromoacetone 
• 92351-15-0 2-amino-1-(prop-2-yn-1-yl)pyridin-1-ium bromide 
• 934-37-2 2-methylimidazo[1,2-a]pyridine 
• 128-08-5 N-Bromosuccinimide 

Downstream Products

• 1246184-22-4 N-(2-chloro-5-(2-methylimidazo[1,2-a]pyridin-3-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide 
• 1345964-72-8 3-(diphenylphosphoryl)-2-methylimidazo[1,2-a]pyridine hydrochloride 
• 1366591-20-9 2-methyl-3-(o-tolyl)imidazo[1,2-a]pyridine 
• 1345964-75-1 3-(hydroxydiphenylmethyl)-1,2-dimethylimidazo[1,2-a]-pyridin-1-ium trifluoroacetate 
• 1345964-73-9 (2-methylimidazo[1,2-a]pyridin-3-yl)diphenylmethanol 
• 1345964-66-0 3-(diphenylphosphorothioyl)-2-methylimidazo[1,2-a]pyridine hydrochloride 
• 1128191-81-0 4-chloro-3-(2-methylimidazo[1,2-a]pyridin-3-yl)aniline 

Relevant articles and documents

Ultrasound-Promoted and Base-Mediated Regioselective Bromination of Imidazo[1,2- a ]pyridines with Pyridinium Tribromide

By using pyridinium tribromide as the bromo source, an efficient- and practical protocol for the synthesis of C3-brominated imidazo-[1,2- a ]pyridines through ultrasound-promoted and Na 2CO 3-mediated regioselective bromination of im

Chemodivergent synthesis of: N -(pyridin-2-yl)amides and 3-bromoimidazo[1,2- a] pyridines from α-bromoketones and 2-aminopyridines

N-(Pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines were synthesized respectively from α-bromoketones and 2-aminopyridine under different reaction conditions. N-(Pyridin-2-yl)amides were formed in toluene via C-C bond cleavage promoted by I2/s

Transition-metal-free regioselective C-H halogenation of imidazo[1,2-: A] pyridines: Sodium chlorite/bromite as the halogen source

A facile transition-metal-free regioselective halogenation of imidazo[1,2-a]pyridines using sodium chlorite/bromite as the halogen source is presented. The reaction has provided an efficient method for the formation of C-Cl or C-Br bonds to synthesize 3-c