1094754-90-1

Basic information

• Product Name: 3-Bromo-6-fluoroindole
• Synonyms: 3-Bromo-6-fluoroindole;3-broMo-6-fluoro-1H-indole
• CAS NO: 1094754-90-1
• Molecular Formula: C₈H₅BrFN
• Molecular Weight: 214.0344032
• Mol File: 1094754-90-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Bromo-6-fluoroindole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-6-fluoroindole(1094754-90-1)
• EPA Substance Registry System: 3-Bromo-6-fluoroindole(1094754-90-1)

Safety Data

• Hazardous Substances Data: 1094754-90-1(Hazardous Substances Data)

Usage

General Description

3-Bromo-6-fluoroindole is a chemical compound that belongs to the class of indole derivatives. It is a heterocyclic aromatic compound containing a five-membered ring with two carbon atoms, three nitrogen atoms, and one bromine and one fluorine atom. 3-Bromo-6-fluoroindole is mainly used as a building block in organic synthesis to create pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable intermediate in the production of various compounds with potential medicinal and agricultural applications. Additionally, 3-Bromo-6-fluoroindole has been studied for its potential biological activities, including antifungal and antibacterial properties.

Upstream product

• 399-51-9 6-fluoro-1H-indole 

Relevant articles and documents

Five-membered heterocyclic oxo carboxylic acid compound and medical application thereof

The invention relates to a five-membered heterocyclic oxo carboxylic acid compound and a medical application thereof. Specifically, the invention relates to a compound, a pharmaceutical salt, a prodrug, a hydrate, a solvate or a crystal form as shown in a formula (I), and also relates to a preparation method of the compound, a pharmaceutical composition containing the compound and an application of the pharmaceutical composition as a secretion regulator of interferon type I, especially as an STING agonist in preparation of medicines for preventing and/or treating I-type interferon related diseases.

Suzuki-Miyaura cross-coupling reaction of naphthyl triflate with indole boronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium complex catalyst: Synthesis of naphthalene-linked bis-heterocycles

In this study, the Suzuki-Miyaura cross-coupling reaction of naphthyl triflate with indole boronic acids catalyzed by a recyclable polymer-supported Pd-NHC complex catalyst is presented. The polymer-supported catalyst can be reused several times retaining high activity for the transformation. The structures of all the synthesized compounds were established by elemental analysis and from their mass, 1H-NMR, and 13C-NMR spectra.