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2,2-dichloro-N-(4-ethoxyphenyl)acetamide is a chemical compound with the molecular formula C10H11Cl2NO3. It is an amide derivative, characterized by the presence of an amide group (-CONH-) and a 4-ethoxyphenyl group attached to the nitrogen atom. The compound features two chlorine atoms attached to the carbon atom adjacent to the amide group, which contributes to its reactivity and stability. This organic compound has potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique structure and properties. However, it is essential to handle 2,2-dichloro-N-(4-ethoxyphenyl)acetamide with care, as it may have toxic effects and requires proper safety measures during its synthesis and use.

4202-64-6

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4202-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4202-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4202-64:
(6*4)+(5*2)+(4*0)+(3*2)+(2*6)+(1*4)=56
56 % 10 = 6
So 4202-64-6 is a valid CAS Registry Number.

4202-64-6Downstream Products

4202-64-6Relevant academic research and scientific papers

Approach for the direct synthesis of β-dichlorosubstituted acetanilides using iodine trichloride (ICl3) as the oxidant and catalyst

Zhang, Qing,Liu, Weibing,Chen, Cui,Tan, Liquan

supporting information, p. 453 - 455 (2013/08/25)

A reliable method for direct synthesis of β-dichlorosubstituted acetanilides is reported. The key transformation involves the oxidative and catalytic cleavage of a carbon-carbon bond in the presence of iodine trichloride (ICl3). In this protoco

Organic synthesis using (diacetoxyiodo)benzene (DIB): Unexpected and novel oxidation of 3-oxobutanamides to 2,2-dihalo-N-phenylacetamides

Liu, Wei-Bing,Chen, Cui,Zhang, Qing,Zhu, Zhi-Bo

supporting information; experimental part, p. 344 - 348 (2012/05/04)

A novel and reliable method for the direct preparation of 2,2-dihalo-N-phenylacetamides is reported. The key transformation involves the cleavage of a carbon-carbon bond in the presence of DIB and a Lewis acid as the halogen source, and thus this method s

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