885275-77-4

Basic information

• Product Name: 5-BROMO-IMIDAZO[1,5-A]PYRIDINE
• Synonyms: 5-BROMO-IMIDAZO[1,5-A]PYRIDINE
• CAS NO: 885275-77-4
• Molecular Formula: C7H5BrN2
• Molecular Weight: 197.03
• Mol File: 885275-77-4.mol

Chemical Properties

• Appearance: /
• Density: 1.69g/cm³
• Refractive Index: 1.688
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 5-BROMO-IMIDAZO[1,5-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-IMIDAZO[1,5-A]PYRIDINE(885275-77-4)
• EPA Substance Registry System: 5-BROMO-IMIDAZO[1,5-A]PYRIDINE(885275-77-4)

Safety Data

• Hazardous Substances Data: 885275-77-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-BROMO-IMIDAZO[1,5-A]PYRIDINE is used as a key intermediate in the synthesis of a variety of organic compounds. Its unique structure allows for the creation of new molecules with potential applications in various fields.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 5-BROMO-IMIDAZO[1,5-A]PYRIDINE is utilized as a building block for the development of biologically active compounds. Its incorporation into drug molecules can enhance their therapeutic effects and target specific biological pathways.
Used in Antifungal and Antibacterial Applications:
5-BROMO-IMIDAZO[1,5-A]PYRIDINE demonstrates potential as an antifungal and antibacterial agent. It is used in the development of new antimicrobial drugs to combat resistant strains and improve treatment options for various infections.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, 5-BROMO-IMIDAZO[1,5-A]PYRIDINE is employed to form complexes with metal ions. These complexes have potential applications in catalysis, materials science, and as sensors.
Used in Metal-Catalyzed Reactions:
In the field of catalysis, 5-BROMO-IMIDAZO[1,5-A]PYRIDINE serves as a ligand to modify the properties of metal catalysts, enhancing their efficiency and selectivity in various chemical reactions.

InChI:InChI=1/C7H5BrN2/c8-7-3-1-2-6-4-9-5-10(6)7/h1-5H

Relevant articles and documents

Synthesis and Characterization of Axially Chiral Imidazoisoquinolin-2-ylidene Silver and Gold Complexes

The selective Suzuki cross-coupling of 1,3-dichloroisoquinoline with 2-substituted 1-naphthylboronic acids/esters followed by construction of the imidazo[1,5-b]isoquinoline ring and alkylation constitutes a straightforward route to imidazolium salts fused into an axially chiral biaryl skeleton. Metalation of these azolium salts afforded the corresponding NHC silver complexes, which were used as carbene transfer agents for the synthesis of Au(I) derivatives.

FUSED HETEROCYCLIC DERIVATIVES, THEIR PREPARATION METHODS THEREOF AND MEDICAL USES THEREOF

The present invention relates to fused heterocyclic derivatives, processes for their preparation and their use in medicine. Specifically, the present invention relates to a novel derivative represented by the formula (I′), or its pharmaceutically acceptable salt thereof, a pharmaceutical composition containing the derivative or its pharmaceutically acceptable salt thereof, and the method for preparing the derivative and its pharmaceutically acceptable salt thereof. The present invention also relates to the use of the derivative and its pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing the derivative and its pharmaceutically acceptable salt thereof in the preparation of medicines, in particularly as IDO inhibitor medicines, for treating and/or preventing cancers. Wherein each substituent of the formula (I′) is the same as defined in the specification.