878198-71-1

Basic information

• Product Name: 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE;Imidazo[1,2-a]pyridine, 2-(chloromethyl)-5-fluoro-
• CAS NO: 878198-71-1
• Molecular Formula: C₈H₆ClFN₂
• Molecular Weight: 184.5980432
• EINECS: 200-589-5
• Mol File: 878198-71-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE(878198-71-1)
• EPA Substance Registry System: 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE(878198-71-1)

Safety Data

• Hazardous Substances Data: 878198-71-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly for the development of drugs targeting neurological disorders and cancer. Its unique structure allows for the creation of new molecules with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE is utilized as a precursor in the development of new agrochemicals, contributing to the advancement of crop protection and management solutions.
It is important to handle and use 2-(CHLOROMETHYL)-5-FLUOROIMIDAZO[1,2-A]PYRIDINE with caution due to its potential hazardous properties, ensuring safety in both research and industrial applications.

Upstream product

• 1597-32-6 6-fluoro-pyridin-2-ylamine 
• 534-07-6 1,3-Dichloroacetone 

Downstream Products

• 878198-72-2 (8R)-N-[(5-fluoroimidazo[1,2-a]pyridin-2-yl)methyl]-N-{(1R)-1-[4-(methyloxy)phenyl]ethyl}-5,6,7,8-tetrahydro-8-quinolinamine 

Relevant articles and documents

Synthesis of a novel tricyclic 1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline ring system and CXCR4 antagonists with potent activity against HIV-1

Stereorandom and diastereoselective syntheses of a novel 1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline ring system are described. Derivatives of all four diastereomers were prepared and isolated in >98% ee. The pure enantiomers were compared in order t

CHEMICAL COMPOUNDS

There is provided novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as C

CHEMICAL COMPOUNDS

The present invention provides novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a recep

CHEMICAL COMPOUNDS

The present invention provides compounds of Formula (I) comprising: including salts, solvates, and physiologically functional derivatives thereof, pharmaceutical formulations containing them, processes for their preparation, and methods of treatment using them.