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916203-59-3

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916203-59-3 Usage

Chemical Class

Naphthyridinone

Explanation

The compound belongs to the naphthyridinone class, which is a group of heterocyclic compounds with a naphthyridine ring structure.

Explanation

It is a heterocyclic compound, meaning it contains a ring of atoms with at least one atom being different from carbon.

Explanation

The compound has a naphthyridine ring structure, which is a type of fused-ring system containing nitrogen atoms.

Explanation

The compound has a 5-chloro-1-(2,6-dichlorophenyl) substituent attached to the naphthyridine ring, which contributes to its chemical properties and potential applications.

Explanation

It is used in the pharmaceutical industry as a potential drug candidate for various therapeutic applications due to its unique chemical structure and properties.

Explanation

The compound has been studied for its potential antifungal properties, which could make it useful in treating fungal infections.

Explanation

It has also been studied for its potential antibacterial properties, which could lead to its use in treating bacterial infections.

Explanation

The compound may have applications in the treatment of cancer due to its unique chemical structure and potential biological activities.

Explanation

It may also have potential applications in the treatment of other diseases, as further research is ongoing to explore its medicinal uses.

Explanation

Further research is being conducted to explore the potential medicinal uses of 1,6-Naphthyridin-2(1H)-one, 5-chloro-1-(2,6-dichlorophenyl)-, as its full range of applications and properties are not yet fully understood.

Heterocyclic Compound

Yes

Ring Structure

Naphthyridine

Substituent

5-chloro-1-(2,6-dichlorophenyl)

Pharmaceutical Industry

Potential drug candidate

Antifungal Properties

Potential

Antibacterial Properties

Potential

Cancer Treatment

Possible application

Other Disease Treatments

Possible application

Ongoing Research

Yes

Check Digit Verification of cas no

The CAS Registry Mumber 916203-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,2,0 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 916203-59:
(8*9)+(7*1)+(6*6)+(5*2)+(4*0)+(3*3)+(2*5)+(1*9)=153
153 % 10 = 3
So 916203-59-3 is a valid CAS Registry Number.

916203-59-3Relevant articles and documents

Unique tandem heck-lactamization naphthyridinone ring formation between acrylanilides and halogenated pyridines

Cvetovich, Raymond J.,Reamer, Robert A.,DiMichele, Lisa,Chung, John Y. L.,Chilenski, Jennifer R.

, p. 8610 - 8613 (2007/10/03)

The Heck coupling of acrylanilides with 4-bromo-2-chloro-3-iodo-pyridine using palladium acetate can produce bis-Heck products or undergo an unusual tandem Heck-lactamization ring formation to generate 5-chloro-1-aryl-1,6- naphthyridin-2(1H)-ones.

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