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7,8-difluoroquinolin-3-amine is a quinoline derivative with the molecular formula C9H6F2N2, featuring two fluorine atoms and an amine group. This chemical compound has potential applications in the pharmaceutical industry, particularly in the development of new drugs or therapeutic compounds. Its unique structure and chemical properties make it suitable for use as a building block in organic synthesis. Additionally, 7,8-difluoroquinolin-3-amine may also have potential biological activities that could be of interest for further research and development in the field of medicinal chemistry.
Used in Pharmaceutical Industry:
7,8-difluoroquinolin-3-amine is used as a building block in organic synthesis for the development of new drugs or therapeutic compounds due to its unique structure and chemical properties.
Used in Medicinal Chemistry Research:
7,8-difluoroquinolin-3-amine is used as a subject of research for potential biological activities, which could lead to further advancements in the field of medicinal chemistry.

318685-32-4

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318685-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 318685-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,8,6,8 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 318685-32:
(8*3)+(7*1)+(6*8)+(5*6)+(4*8)+(3*5)+(2*3)+(1*2)=164
164 % 10 = 4
So 318685-32-4 is a valid CAS Registry Number.

318685-32-4Downstream Products

318685-32-4Relevant academic research and scientific papers

3-amino -7,8-difluoro-quinoline and wherein the intermediate synthesis method

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Paragraph 0026; 0027; 0028, (2016/10/10)

The invention provides 3-amino-7,8-difluoroquinoline and a synthesis method of an intermediate body of the 3-amino-7,8-difluoroquinoline. 3-amino-7,8-difluoromethylquinoline is prepared by three steps of carrying out substitution reaction on 7,8-difluoroquinoline, carrying out condensation reaction on 3-bromine-7,8-difluoroquinoline and carrying out amino deprotection reaction on 7,8-difluoro-3-tertoxy carbonyl amino quinoline; 7,8-difluoroquinoline-3-formic acid is prepared by three steps of carrying out substitution reaction on 7,8-difluoroquinoline, carrying out carbonyl insertion reaction on 3-bromine-7,8-difluoroquinoline and carrying out hydrolysis reaction on 7,8-difluoroquinoline-3-methyl formate. The synthesis method of the intermediate body of 3-amino-7,8-difluoroquinoline is simple in route, high in total yield, convenient to operate, simple in post-treatment, free of poisonous reagent and suitable for large-scale production.

Benzo[f]naphthyridine derivatives, their preparation and compositions containing them

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, (2008/06/13)

Benzo[f]naphthyridine derivatives of formula (I): benzo[f]naphthyridine derivatives and benzo[f]naphthyridine esters of formula (IVa): aminoquinoline derivatives of formula (X): processes for preparing such compounds; and compositions comprising them.

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