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3-(2-chlorophenylamino)-N,N-dimethylpropionamide is a chemical compound with the molecular formula C11H14ClNO. It is an amide derivative, characterized by the presence of an amide functional group (-CONH-) and a 2-chlorophenylamine moiety. 3-(2-chlorophenylamino)-N,N-dimethylpropionamide is a white to off-white crystalline solid and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its potential applications in the chemical industry, it is essential to handle 3-(2-chlorophenylamino)-N,N-dimethylpropionamide with care, as it may have toxicological properties and requires proper safety measures during its use and disposal.

1950-43-2

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1950-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1950-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1950-43:
(6*1)+(5*9)+(4*5)+(3*0)+(2*4)+(1*3)=82
82 % 10 = 2
So 1950-43-2 is a valid CAS Registry Number.

1950-43-2Downstream Products

1950-43-2Relevant academic research and scientific papers

Method for catalyzing amino protection by imidazole hydrochloride

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Paragraph 0039-0043, (2019/08/01)

The invention provides an amino protection method which realizes multi-substituted amino protection by using imidazole hydrochloric acid as an accelerator to push derivatives of primary amine, secondary amine and acrylamide to perform Michael addition at a relatively low temperature, wherein the imidazole hydrochloric acid promotes a carbon-nitrogen bond to crack back to the derivatives of primaryamine and acrylamide at a high temperature. The method provided by the invention is simple and economical, high in practicability, free of any other catalysts or additives, capable of protecting amino to have good functional group tolerance and excellent yield and purity, short in reaction time, free from harsh reaction conditions and suitable for industrial production.

Michael addition reaction catalyzed by imidazolium chloride to protect amino groups and construct medium ring heterocycles

Dai, Zeshu,Li, Dan,Li, Yanwu,Li, Zhiyao,Luo, Wen,Shang, Suqin,Tian, Qingqiang,Wang, Xuetong,Yuan, Jianyong,Zhang, Ying

supporting information, (2019/12/04)

An effective approach for amino protection and construction of a seven-membered ring has been developed. The method uses imidazolium chloride to carry out the Michael addition reaction at low temperatures and perform amino deprotection or construction of a seven-membered ring at high temperatures.

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