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3-Amino-4-phenethylamino-benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

445466-23-9

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445466-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 445466-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,4,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 445466-23:
(8*4)+(7*4)+(6*5)+(5*4)+(4*6)+(3*6)+(2*2)+(1*3)=159
159 % 10 = 9
So 445466-23-9 is a valid CAS Registry Number.

445466-23-9Relevant academic research and scientific papers

A concise synthesis of 2-(2-aminothiophene)-benzimidazoles by one-pot multicomponent reaction

Chen, Li-Hsun,Chuang, Ying-Sheng,Narhe, Bharat D.,Sun, Chung-Ming

, p. 13934 - 13943 (2013)

A one-pot synthesis of 2-aminothiophene linked benzimidazoles was achieved by utilizing 2-cyanomethyl benzimidazoles in a modified Gewald multicomponent reaction. The synthetic strategy of the reaction involved treatment of 2-(cyanomethyl)-benzimdazole wi

A Novel Mechanistic Study on Ultrasound-Assisted, One-Pot Synthesis of Functionalized Benzimidazo[2,1-b]quinazolin-1(1H)-ones

Chen, Li-Hsun,Chung, Tsai-Wen,Narhe, Bharat D.,Sun, Chung-Ming

, p. 162 - 169 (2016/03/25)

Ultrasound-assisted synthesis of benzimidazo[2,1-b]quinazolin-1(1H)-ones was achieved via piperidine-catalyzed three-component reaction of 2-aminobenzimidazoles, an aromatic aldehyde, and 1,3-dione in aqueous isopropanol. This mechanism was first suspected following our identification of unusual reaction intermediates in a one-pot reaction. An unprecedented coupling reaction, it involved a nucleophilic attack by 2-aminobenzimidazole on in situ generated Michael adduct, followed by electrocyclic ring formation reaction. In contrast to the commonly accepted mechanism, that the direct reaction of 2-amino benzimidazole with a Knoevenagel adduct cannot deliver target compounds.

A facile IL-DMSO assisted synthesis of 5-, 6-, and 7-membered benzo-annelated cyclic guanidines

Verma, Amit,Giridhar, Rajani,Modh, Pratik,Yadav, Mange Ram

, p. 2954 - 2958 (2012/07/28)

A new and facile IL-DMSO assisted method has been developed for the synthesis of biologically important cyclic guanidines like 2-aminobenzimidazole, 2-imino-4-quinazolinone, and 2-imino-5-benzotriazepinones at ambient temperatures. The desired products could be obtained by microwave irradiation32 also, but at elevated temperatures. A plausible mechanism for catalysis has been proposed.

Construction of a Stable Flavin-Gold Electrode displaying Very Fast Electron Transfer Kinetics

Edwards, Timothy R. G.,Cunnane, Vincent J.,Parsons, Roger,Gani, David

, p. 1041 - 1043 (2007/10/02)

The bis-phenylthiourea phenethylisoalloxazine (6) was synthesised and was attached to the gold through its thiourea side-chains; cyclic voltammetric investigation of the redox properties of the system confirmed that the flavin was a stable adsorbed species and revealed that electron transfer between the conductor and the flavin was very fast.

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