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2-(o-Chlorobenzamide)benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56642-91-2

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56642-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56642-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56642-91:
(7*5)+(6*6)+(5*6)+(4*4)+(3*2)+(2*9)+(1*1)=142
142 % 10 = 2
So 56642-91-2 is a valid CAS Registry Number.

56642-91-2Downstream Products

56642-91-2Relevant academic research and scientific papers

SYNTHESIS OF 4-ARYL BENZIMIDAZOLO-s-TRIAZIN-2-ONES AND 2-AROYLAMINOBENZIMIDAZOLO-1,2,4-THIADIAZOLINES

Sridevi, G.,Rao, P. Jayaprasad,Reddy, K. Kondal

, p. 965 - 972 (2007/10/02)

Reaction of 2-aminobenzimidazole with aroylisothiocyanates gave 2-aroylaminobenzimidazoles (3) and N-aroyl-N'-(benzimidazol-2-yl)-thioureas (4).The products obtained on reaction of 4 with PCl5 in POCl3 , and with oxidising agents have been identified as 4

2-PHENYL- AND 2-BENZAMIDO-BENZIMIDAZOLES

Sluka, Jaroslav,Danek, Jaroslav,Bedrnik, Petr,Budesinsky, Zdenek

, p. 2703 - 2708 (2007/10/02)

2-Phenylbenzimidazoles I-VI with chlorine atom or methoxy group on the benzene ring were prepared by a modified method.Acylation of 2-aminobenzimidazoles with substituted benzoyl chlorides afforded the 2-benzamidobenzimidazoles VII-XXXVI.All these compounds were tested for anthelmintic and coccidiostatic activity.

Reactions with N-Acylimino-dithiocarbonic-acid-diesters

Augustin, M.,Richter, M.,Salas, S.

, p. 55 - 68 (2007/10/02)

Reactions of N-acylimino-dithiocarbonic-acid-S,S-diesters 1 with nucleophilic compounds present new possibilities to synthesize heterocycles.With amines 1a reacts by mono- and disubstitution, respectively, of methylthio-groups to isothioureas 2 and guanidines 3, with 1,2-binucleophilic arenes to benzoheterocycles 4, with aliphatic diamines to imidazolines 5, pyrimidines 6, diazepines 7 and the hexamethylene-diamine-derivatives 8. 1a reacts also with hydrazines to 1,2,4-triazoles 9 and with hydrazides to the thiosemicarbazones 10 or 1,3,4-oxadiazoles 11.Heterocyclisations of 1 with guanidines, thiourea, salts of thiourea and amidines give the 1,3,5-triazines 12, 14, 15 and 16.N-benzoyl-dithiocarbonic-acid-methylester -amid reacts with CH-acidic compounds to thiazoles 17.The structures of the final products are determined by i.r.-, 1H-n.m.r.-, u.v.- and mass-spectras.

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