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Diethyl 1,4-phenylenebis(methylene)dicarbamate, also known as Kepone, is a synthetic organochlorine compound with the chemical formula C16H18N2O4. It was primarily used as a pesticide in the 1960s and 1970s, targeting insects and mites. Kepone is highly toxic and persistent in the environment, leading to its ban in the United States in 1978 due to its potential to cause cancer, reproductive issues, and other health problems in humans and wildlife. Its chemical structure consists of a central phenylene ring with two methylene groups connecting it to two carbamate groups, which are derived from diethylamine. The compound's persistence and toxicity have made it a subject of significant environmental and health concerns, highlighting the need for strict regulation of such chemicals.

4182-40-5

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4182-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4182-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4182-40:
(6*4)+(5*1)+(4*8)+(3*2)+(2*4)+(1*0)=75
75 % 10 = 5
So 4182-40-5 is a valid CAS Registry Number.

4182-40-5Downstream Products

4182-40-5Relevant academic research and scientific papers

N-Substituted carbamate synthesis using urea as carbonyl source over TiO2-Cr2O3/SiO2 catalyst

Wang, Peixue,Ma, Yubo,Liu, Shimin,Zhou, Feng,Yang, Benqun,Deng, Youquan

, p. 3964 - 3971 (2015)

The use of urea as an active form of carbon dioxide is a feasible way to substitute phosgene in the chemical industry. This paper reports an effective route for the synthesis of N-substituted carbamates from amines, urea and alcohols. Under the optimized reaction conditions, several important N-substituted carbamates were successfully synthesized in 95-98% yields over a TiO2-Cr2O3/SiO2 catalyst. The catalyst could be reused for several runs without deactivation. The catalysts were characterized by BET, XPS, XRD, and TPD, which suggested that the strength and amount of the acidic and basic sites might be the major reason for the high catalytic activity of TiO2-Cr2O3/SiO2.

Synthesis, molecular structure of diethyl phenylenebis(methylene)dicarbamates and FTIR spectroscopy molecular recognition study with benzenediols

Saucedo-Balderas, Marlene M.,Delgado-Alfaro, Rogelio A.,Martínez-Martínez, Francisco J.,Ortegón-Reyna, David,Bernabé-Pineda, Margarita,Zú?iga-Lemus, Oscar,González-González, Juan S.

, (2015/03/05)

The synthesis, density functional theory (DFT) molecular structure and Fourier transform infrared spectroscopy (FTIR) molecular recognition study of diethyl phenylenebis(methylene)dicarbamates with 1,2- and 1,3-benzenediols is described. The formation of

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