1198413-17-0

Basic information

• Product Name: 7-Bromo-4-hydroxy-[1,8]naphthyridine
• Synonyms: 7-Bromo-4-hydroxy-[1,8]naphthyridine;7-BroMo-1,8-naphthyridin-4(1H)-one
• CAS NO: 1198413-17-0
• Molecular Formula: C8H5BrN2O
• Molecular Weight: 225.0421
• Mol File: 1198413-17-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-Bromo-4-hydroxy-[1,8]naphthyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Bromo-4-hydroxy-[1,8]naphthyridine(1198413-17-0)
• EPA Substance Registry System: 7-Bromo-4-hydroxy-[1,8]naphthyridine(1198413-17-0)

Safety Data

• Hazardous Substances Data: 1198413-17-0(Hazardous Substances Data)

Usage

General Description

7-Bromo-4-hydroxy-[1,8]naphthyridine is a chemical compound that belongs to the naphthyridine class of compounds. It is characterized by its molecular structure, which consists of a naphthyridine ring with a hydroxyl group at the 4th position and a bromine atom at the 7th position. 7-Bromo-4-hydroxy-[1,8]naphthyridine has potential applications in the field of medicinal chemistry, particularly as a building block for the synthesis of pharmaceutical drugs. It may also have biological activities, making it a subject of interest for research in pharmacology and drug discovery. Additionally, 7-Bromo-4-hydroxy-[1,8]naphthyridine may be used as a reagent in organic synthesis. Please note that this is a hypothetical chemical compound and should not be considered factual without proper verification.

Upstream product

• 1198412-96-2 C₁₂H₁₁BrN₂O₄ 

Relevant articles and documents

Synthesis of halogenated 4H-pyrido[1,2-a]pyrimidin-4-ones

Halogenated 4H-pyrido[l,2-a]pyrimidin-4-one were synthesized by thermal cyclization and decarboxylation of isopropylidene (2-pyridylamino)methylenemalonates, prepared from 2-aminopyridines and isopropylidene methoxymethylenemalonate formed in situ. Instead of 4H-pyrido[l,2-a]pyrimidin-4-ones, the 6-chloro and 6-bromo derivatives afforded mixtures of 7-halo-l,4-dihydro-l,8-naphthyridin-4-ones and 1-(6-halo-2-pyridyl)-3-[(6-halo-2-pyridylamino)methylene]-1,2,3,4-tetrahydropyridine-2,4-diones. The latters formed from N-(2-pyridyl)iminoketenes, the common intermediates of 4H-pyrido[l,2-a]pyrimidin-4-one and l,8-naphthyridin-4-ones, via a "head-to-tail" [4+2] cycloaddition. 3-Halo-4H-pyrido[l,2-a]pyrimidin-4-ones were obtained from 4H-pyrido[1,2-a]pyrimidin-4-one with N-halosuccinimides. The structures of the new compounds were characterized by means of 1H NMR and 13C NMR examinations.