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rac-1,3-dimethyl-4,5-diphenylimidazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86932-59-4

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86932-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86932-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,3 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86932-59:
(7*8)+(6*6)+(5*9)+(4*3)+(3*2)+(2*5)+(1*9)=174
174 % 10 = 4
So 86932-59-4 is a valid CAS Registry Number.

86932-59-4Downstream Products

86932-59-4Relevant academic research and scientific papers

Synthesis of Imidazolinium Salts by Pd/C-Catalyzed Dehydrogenation of Imidazolidines

Ando, Shin,Ishizuka, Tadao,Xiao, Bowen

supporting information, p. 4551 - 4554 (2021/08/30)

A method for the synthesis of imidazolinium salts through a catalytic dehydrogenation was developed using Pd/C as a catalyst with ammonium salt as an additive. Optimization of the reaction conditions revealed the existence of a proton source that was necessary to accomplish the reaction. Under the optimal conditions, oxidation-sensitive components, such as an allyl, a furan, and a thiophene can be introduced into the corresponding imidazolinium salts. In addition to the varied N-substituents, the presented method can be used to synthesize a series of 2-substituted imidazolinium salts.

Indium trichloride: A versatile catalyst for the synthesis of fully saturated imidazoles

Kidwai, Mazaahir,Poddar, Priya Roona,Singhal, Kavita

experimental part, p. 886 - 892 (2009/12/24)

Ketimines are readily reduced to corresponding vicinal diamines using InCl3 and zinc followed by simple cyclization to fully saturated imidazoles with various aldehydes. InCl3 has been found to play an efficient catalytic role for th

Preparation and properties of nitrogen-substituted thiosulfinyl compounds and related new heterocycles

Yoshida, Sanae,Sugihara, Yoshiaki,Nakayama, Juzo

, p. 8116 - 8119 (2008/03/13)

The reaction of dilithiated N,N′-dimethyl-1,2-diphenylethylenediamine with disulfur dichloride (S2Cl2) gave a thiosulfinyl compound (R2N)2S{double bond, long}S, 2,5-dimethyl-3,4-diphenyl-1,2,5-thiadiazolidine 1-sulfide, whereas the treatment of dilithiated N,N′-bis(p-toluenesulfonyl)-1,2-diphenylethylenediamine with S2Cl2 furnished a new heterocycle, 3,6-bis(p-toluenesulfonyl)-4,5-diphenyl-4H,5H-1,2,3,6-dithiadiazine.

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