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1-Butanone, 1-(2-amino-5-chlorophenyl)-, also known as 1-(2-amino-5-chlorophenyl)butan-1-one, is an organic compound with the chemical formula C10H12ClNO. It is a derivative of butanone, featuring a 2-amino-5-chlorophenyl group attached to the carbonyl carbon. 1-Butanone, 1-(2-amino-5-chlorophenyl)- is characterized by its molecular weight of 197.66 g/mol and a melting point of 47-48°C. It is a colorless to pale yellow solid and is soluble in organic solvents. 1-Butanone, 1-(2-amino-5-chlorophenyl)-, is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chlorinated compounds. Due to its potential applications and chemical properties, it is important to handle 1-Butanone, 1-(2-amino-5-chlorophenyl)- with care, as it may have toxic effects and should be stored away from heat and open flames.

1685-21-8

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1685-21-8 Usage

Structure

A derivative of butanone (methyl ethyl ketone) with an added amino group and a chlorophenyl group.

Usage

In organic synthesis and pharmaceutical research as a building block for more complex molecules.

Applications

In the development of pharmaceuticals and agrochemicals.

Research potential

Unique structure and properties make it a potential candidate for further research in the fields of medicinal chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1685-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1685-21:
(6*1)+(5*6)+(4*8)+(3*5)+(2*2)+(1*1)=88
88 % 10 = 8
So 1685-21-8 is a valid CAS Registry Number.

1685-21-8Relevant academic research and scientific papers

Control of parasites in animals by the use of novel trifluoromethanesulfonanilide oxime ether derivatives

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Page/Page column 33; 8/12, (2010/10/20)

Novel trifluoromethanesulfonanilide oxime ether compounds useful for controlling endo and/or ectoparasites in the environment are provided, together with methods of making the same, and methods of using the inventive compounds to treat parasite infestations in vivo or ex vivo.

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