642478-16-8

Basic information

• Product Name: 1,4-Dioxino[2,3-f]quinolin-10(7H)-one, 9-chloro-2,3-dihydro-
• Synonyms: 1,4-Dioxino[2,3-f]quinolin-10(7H)-one, 9-chloro-2,3-dihydro-
• CAS NO: 642478-16-8
• Molecular Formula: C11H8ClNO3
• Molecular Weight: 237.64
• Mol File: 642478-16-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-Dioxino[2,3-f]quinolin-10(7H)-one, 9-chloro-2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dioxino[2,3-f]quinolin-10(7H)-one, 9-chloro-2,3-dihydro-(642478-16-8)
• EPA Substance Registry System: 1,4-Dioxino[2,3-f]quinolin-10(7H)-one, 9-chloro-2,3-dihydro-(642478-16-8)

Safety Data

• Hazardous Substances Data: 642478-16-8(Hazardous Substances Data)

Usage

Chemical Class

Dioxinoquinolones

Explanation

The compound belongs to a class of heterocyclic compounds known as dioxinoquinolones.

Explanation

The unique molecular structure of the compound consists of a dioxane ring fused to a quinolin-10-one ring system, which contributes to its chemical properties.

Explanation

The presence of a chlorine atom in the 9th position of the 2,3-dihydro-quinoline part of the molecule gives the compound its characteristic properties and influences its reactivity.

Explanation

The compound has potential applications in medicinal chemistry, either as a pharmacophore or as a structural motif in the development of new drugs with diverse biological activities.

Explanation

Due to its molecular structure and the presence of a chlorine atom, the compound may exhibit reactivity, which should be considered when handling or using it in chemical reactions.

Explanation

The compound may have toxic properties, and it is important to handle it with care to minimize the risk of exposure or harm to humans and the environment.

Explanation

Given its potential reactivity and toxicity, it is crucial to follow proper handling procedures and safety precautions when working with this chemical compound.

Molecular Structure

Dioxane ring fused to a quinolin-10-one ring system

Chlorine Substitution

9-chloro at the 2,3-dihydro-quinoline moiety

Potential Applications

Medicinal chemistry

Reactivity

Potential reactivity

Toxicity

Potential toxicity

Handling Precautions

Careful handling required

Upstream product

• 872714-67-5 2,3-dihydro-7H-[1,4]dioxino[2,3-f]quinolin-10-one 

Relevant articles and documents

ANTIBACTERIAL AGENTS

Naphthalene, quinoline, quinoxaline and naphthyridine derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.