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2-p-toluidino-ethanethiol, also known as 2-(4-methylphenyl)ethylmercaptan, is an organic compound with the chemical formula C9H13NS. It is a colorless to pale yellow liquid with a strong, pungent odor. 2-p-toluidino-ethanethiol is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its two functional groups: an ethanethiol (mercaptan) group and a p-toluidine (4-methylaniline) group. The presence of these functional groups allows for a wide range of chemical reactions and applications, making 2-p-toluidino-ethanethiol a versatile building block in the chemical industry.

5978-00-7

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5978-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5978-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5978-00:
(6*5)+(5*9)+(4*7)+(3*8)+(2*0)+(1*0)=127
127 % 10 = 7
So 5978-00-7 is a valid CAS Registry Number.

5978-00-7Relevant academic research and scientific papers

An NMR study of the reactions of chlorophosphines with AlCl3. Phosphenium cations featuring a S-P-N linkage

Huang, Tian-Bao,Liu, Ling-Fei,Zhang, Jing-Ling,Xu, Xuang-Long,Huang, Wen-Fang,Chen, Ru-Yu,Wang, Ke,Yu, Xiao-Ming,Liu, Xiao-Peng

, p. 183 - 193 (2007/10/03)

The N-P+-S phosphenium cations 1, 2 and 3 have been prepared by treatment of the respective precursor chlorophosphines 4, 5 and 6 with the stoichiometric quantity of AlCl3 in CH2Cl2 solution. The cations 3 are n

Syntheses de β-sultames (thiazetidines-1,2 dioxyde-1,1)

Champseix, A.,Chanet, J.,Etienne, A.,Berre, A. Lemasson, J. C.,Napierala, C.,Vessiere, R.

, p. 463 - 472 (2007/10/02)

β-sultams (1,2-thiazetidine-1,1-dioxides) are easily prepared by 1-halogensulphonyl-2-aminoalkane cyclisation. Two processes based upon this principle have permitted the preparation of many variously N and C-substituted β-sultams. 1) In the first method 1-chlorosulphonyl-2-aminoalkane hydrochlorides, prepared from taurines or β-aminothiols, cyclised in the presence of base. 2) The second process involves the spontaneous cyclisation of 1-fluorosulphonyl-2-aminoalkanes prepared Michael addition of primary amines to 1-fluorosulphonylethene.

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