209328-99-4

Basic information

• Product Name: 2-Fluoro-3-Bromo-5-Aminopyridine
• Synonyms: 2-Fluoro-3-Bromo-5-Aminopyridine;5-Bromo-6-fluoropyridin-3-amine
• CAS NO: 209328-99-4
• Molecular Formula: C5H4BrFN2
• Molecular Weight: 191.0010632
• Product Categories: Pyridine
• Mol File: 209328-99-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 305℃
• Flash Point: 139℃
• Appearance: /
• Density: 1.813
• Vapor Pressure: 0.000822mmHg at 25°C
• Refractive Index: 1.604
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-Fluoro-3-Bromo-5-Aminopyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Fluoro-3-Bromo-5-Aminopyridine(209328-99-4)
• EPA Substance Registry System: 2-Fluoro-3-Bromo-5-Aminopyridine(209328-99-4)

Safety Data

• Hazardous Substances Data: 209328-99-4(Hazardous Substances Data)

Usage

General Description

2-Fluoro-3-Bromo-5-Aminopyridine is a chemical compound with the molecular formula C5H4BrFN2. It is a pyridine derivative with a fluorine atom at the 2 position, a bromine atom at the 3 position, and an amino group at the 5 position. 2-Fluoro-3-Bromo-5-Aminopyridine is commonly used as a building block in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It is also used as a reagent in the synthesis of various bioactive compounds and pharmaceutical intermediates. The presence of the fluorine and bromine atoms makes 2-Fluoro-3-Bromo-5-Aminopyridine a versatile and useful compound for conducting chemical reactions and producing new molecules with potentially valuable properties.

InChI:InChI=1/C5H4BrFN2/c6-4-1-3(8)2-9-5(4)7/h1-2H,8H2

Upstream product

• 1868-58-2 3-bromo-2-fluoro-5-nitropyridine 
• 5470-17-7 3-bromo-2-chloro-5-nitropyridine 

Relevant articles and documents

FE NANOPARTICLES WITH PPM CONTENTS OF PD, CU AND/OR NI, REACTIONS IN WATER CATALYZED BY THEM

The present application discloses a nanoparticle composition prepared from a mixture comprising: a) a transition metal salt; b) an iron salt; and c) a reducing agent; and methods for the use of such compositions, including the reduction of an organic compound comprising a nitro group to form an organic compound comprising an amine group, the Cu-catalyzed cyclization of an azide and an alkyne (click chemistry) and cross coupling reactions, notably Suzuki-Miyaura reactions. The transition metal salts are in particular Pd, Cu and Ni salts, the content of these metals being typically in the ppm range based on the major constituent Fe in the final products.

3-Pyridyl enantiomers and their use as analgesics

The present invention relates to a method of controlling pain in mammals, including humans, comprising administering to a mammal or patient in need of treatment thereof selected compounds of formula I: STR1 or a pharmaceutically acceptable salt thereof. The invention further relates to selected (R) and (S) compounds of formula I above which are useful as analgesics as well as neuronal cell death preventors and anti-inflammatories.