1082041-10-8

Basic information

• Product Name: 1H-Pyrrolo[3,2-c]pyridine, 7-broMo-4-fluoro-
• Synonyms: 1H-Pyrrolo[3,2-c]pyridine, 7-broMo-4-fluoro-;7-BroMo-4-fluoro-5-azaindole
• CAS NO: 1082041-10-8
• Molecular Formula: C7H4BrFN2
• Molecular Weight: 215.0224632
• Mol File: 1082041-10-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrolo[3,2-c]pyridine, 7-broMo-4-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[3,2-c]pyridine, 7-broMo-4-fluoro-(1082041-10-8)
• EPA Substance Registry System: 1H-Pyrrolo[3,2-c]pyridine, 7-broMo-4-fluoro-(1082041-10-8)

Safety Data

• Hazardous Substances Data: 1082041-10-8(Hazardous Substances Data)

Usage

Heteroaromatic organic compound

A compound containing both aromatic rings and heteroatoms (such as nitrogen or oxygen) in its structure 1H-Pyrrolo[3,2-c]pyridine, 7-bromo-4-fluorocontains a pyrrole ring fused to a pyridine ring, both of which are aromatic, and have nitrogen atoms as heteroatoms.

Pyrrole and pyridine rings

Two heterocyclic rings fused together The pyrrole ring is a five-membered ring with four carbon atoms and one nitrogen atom, while the pyridine ring is a six-membered ring with five carbon atoms and one nitrogen atom. In 1H-Pyrrolo[3,2-c]pyridine, 7-bromo-4-fluoro-, these two rings are fused together.

Bromine and fluorine substituents

Two halogens attached to the compound at specific positions In this case, bromine is attached to the 7th position and fluorine is attached to the 4th position of the compound. These substituents can influence the compound's reactivity, polarity, and other properties.

Potential applications in medicinal chemistry and pharmaceutical research

The compound may exhibit biological activity or be used as a building block for the synthesis of other compounds 1H-Pyrrolo[3,2-c]pyridine, 7-bromo-4-fluorocould be used in the development of new drugs or as an intermediate in the synthesis of other biologically active compounds.

Structure-activity relationships

Studying how the compound's structure affects its biological activity By analyzing the structure of 1H-Pyrrolo[3,2-c]pyridine, 7-bromo-4-fluoroand its potential analogs, researchers can gain insights into how specific structural features contribute to the compound's biological activity, which can help guide the design of new drugs.

Development of new materials and chemical processes

The unique heterocyclic structure of the compound may be useful for creating new materials or chemical reactions The combination of pyrrole and pyridine rings in 1H-Pyrrolo[3,2-c]pyridine, 7-bromo-4-fluorocould lead to the development of novel materials with unique properties or the creation of new chemical processes that take advantage of the compound's reactivity and structure.