296759-29-0

Usage

Uses

Used in Organic Synthesis:
6-IODO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a reagent in organic synthesis for its reactivity and potential utility in various chemical reactions.
Used in Pharmaceutical Research and Development:
6-IODO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a compound in pharmaceutical research and development due to its unique structure and properties, which may contribute to the discovery of new drugs and therapeutic agents.
Used in Specialty Chemicals Production:
6-IODO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a component in the production of specialty chemicals, where its specific properties can be harnessed for various applications.
Used in Agrochemicals Production:
6-IODO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used in the production of agrochemicals, potentially contributing to the development of new pesticides, herbicides, or other agricultural products.
Further study and investigation of 6-IODO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE in the field of organic chemistry are warranted to explore its full potential and unlock new applications in various industries.

Upstream product

• 553-03-7 3,4-dihydro-2(1H)-quinolone 

Downstream Products

• 124467-20-5 2-chloro-6-iodoquinoline 

Relevant academic research and scientific papers

A para-C–H Functionalization of Aniline Derivatives via In situ Generated Bulky Hypervalent Iodinium Reagents

A practical para-C-H functionalization of aniline derivatives has been developed using an in situ generated bulky hypervalent iodinium reagent. Para-iodo, bromo, chloro, nitro, trifluormethyl aniline derivatives can be obtained efficiently, in many cases in 10 min in a transition metal-free manner. Medicinal chemicals or intermediates can be purified without column chromatography or recrystallization, which significantly reduces the waste and simplifies the work-up process.

Bicyclic aromatic substituted pyridone derivative

Disclosed is a compound represented by the formula (I): Wherein R1 and R2 independently represent a hydrogen atom, a lower alkyl group or the like; X1, X2 and X3 independently represent a methine group or a nitrogen atom; Y1 and Y3 independently represent a single bond, —O— or the like; Y2 represents a lower alkylene group or the like; W1 to W4 independently represent a single bond, a methylene group or the like; L represents a single bond, a methylene group or the like; Z1 and Z2 independently represent a single bond, a C1-4 alkylene group or the like; Ar1 represents an aromatic carbocyclic ring or the like; and Ar2 represents a bicyclic aromatic carbocyclic ring or the like. The compound is useful as a pharmaceutical for a central disease, a cardiovascular disease or a metabolic disease.

BICYCLIC AROMATIC SUBSTITUTED PYRIDONE DERIVATIVE

Disclosed is a compound represented by the formula (I): wherein R1 and R2 independently represent a hydrogen atom, a lower alkyl group or the like; X1, X2 and X3 independently represent a methine group or a nitrogen atom; Y1 and Y3 independently represent a single bond, -O- or the like; Y2 represents a lower alkylene group or the like; W1 to W4 independently represent a single bond, a methlene group or the like; L represents a single bond, a methylene group or the like; Z1 and Z2 independently represent a single bond, a C1-4 alkylene group or the like; Ar1 represents an aromatic carbocyclic ring or the like; and Ar2 represents a bicyclic aromatic carbocyclic ring or the like. The compound is useful as a pharmaceutical for a central disease, a cardiovascular disease or a metabolic disease.

Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1

6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.