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N-(2-Acetylphenyl)-2,2-dichloroacetamide is a chemical compound with the molecular formula C10H8Cl2NO2. It is a derivative of acetamide, featuring a 2-acetylphenyl group attached to the nitrogen atom and two chlorine atoms on the carbonyl carbon. N-(2-Acetylphenyl)-2,2-dichloroacetamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a white crystalline solid, and its properties, such as solubility and stability, can be influenced by the presence of the dichloroacetyl group and the acetylphenyl moiety. The compound's synthesis typically involves the reaction of 2-acetylphenylamine with dichloroacetyl chloride, and it is often used as an intermediate in the preparation of more complex molecules.

6140-12-1

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6140-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6140-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6140-12:
(6*6)+(5*1)+(4*4)+(3*0)+(2*1)+(1*2)=61
61 % 10 = 1
So 6140-12-1 is a valid CAS Registry Number.

6140-12-1Downstream Products

6140-12-1Relevant academic research and scientific papers

Electrosynthesis of 3-chloro-1,4-disubstituted-2(1H)-quinolinones and 3,3-dichloro-4-hydroxy-1,4-disubstituted-3,4-dihydro-2(1H)-quinolinones, as well as a new convenient process to dioxindoles

Batanero, Belen,Barba, Fructuoso

, p. 3706 - 3709 (2007/10/03)

Cathodic reduction of N-(2-acyl(or aroyl)phenyl)-2,2,2,-trichloro-N-alkylacetamide at - 1.2 V (vs SCE) under aprotic conditions yields 3-chloro-1,4-disubstituted-2(1H)-quinolinones (1) as the major product. When the reaction is carried out at -0.8 V (vs S

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