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Acetamide, N-acetyl-N-(2-chlorophenyl)-, also known as 2'-chloroacetanilide, is an organic compound with the chemical formula C8H8ClNO. It is a derivative of acetanilide, where one of the hydrogen atoms on the phenyl ring is replaced by a chlorine atom. This white crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, such as herbicides and fungicides. Due to its potential applications and chemical properties, it is important to handle Acetamide, N-acetyl-N-(2-chlorophenyl)- with care, as it may have toxic effects and should be used in accordance with safety guidelines.

6652-40-0

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6652-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6652-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6652-40:
(6*6)+(5*6)+(4*5)+(3*2)+(2*4)+(1*0)=100
100 % 10 = 0
So 6652-40-0 is a valid CAS Registry Number.

6652-40-0Downstream Products

6652-40-0Relevant academic research and scientific papers

A novel synthesis of 2,6-disubstituted and 2,3,6-trisubstituted anilines

Pews,Hunter,Wehmeyer

, p. 7191 - 7194 (2007/10/02)

2,6-Disubstituted and 2,3,6-trisubstituted anilines have been synthesized by a four-step approachy involving the selective reduction of a para halogen of the diacetanilide derivatives utilizing a palladium-on-carbon catalyst and formic acid salts as the in situ hydrogen donor.

Effect of substituents in the formation of diacetanilides

Ayyangar, Nagaraj R.,Srinivasan, Kumar V.

, p. 1292 - 1296 (2007/10/02)

A number of diacetanilides, including some which have not been reported so far, have been synthesized from the corresponding monoacetyl derivatives and characterized by spectral and elemental analyses.A tlc/fid method for the quantitative estimation of the relative amounts of mono- and diacetyl derivatives has been standardized.Linear correlation of the extent of diacetylation with Hammett ?-values of substituents and basicity constants of monoacetyl derivatives has been established.A plausible mechanism for the diacetylation reaction based on experimental observations has been suggested.An explanation for the anomalous behaviour of acetanilides containing electron-withdrawing substituents in the ortho-position has been put forth.

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