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5,6-dimethyl-2-(p-tolyl)-1H-benzo[d]imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70151-41-6

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70151-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70151-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,5 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70151-41:
(7*7)+(6*0)+(5*1)+(4*5)+(3*1)+(2*4)+(1*1)=86
86 % 10 = 6
So 70151-41-6 is a valid CAS Registry Number.

70151-41-6Downstream Products

70151-41-6Relevant academic research and scientific papers

Redox-Neutral Photocatalytic Radical Cascade Cyclization for the Synthesis of CH2CN/CF2COOEt/CF3-Containing Benzo[4,5]imidazo[2,1-a]isoquinolin-6(5 H)-One Derivatives

Liu, Liang,Yang, De-Yong,He, Yan-Hong,Guan, Zhi

, p. 11892 - 11901 (2020/10/23)

A novel method for the synthesis of benzo[4,5]imidazo[2,1-A]isoquinolin derivatives via visible-light-induced radical cascade cyclization is described. By using N-methacryloyl-2-phenylbenzoimidazoles and diverse radical precursors, various benzo[4,5]imidazo[2,1-A]isoquinolin derivatives containing CH2CN/CF2COOEt/CF3 can be formed in good to excellent yields under mild reaction conditions. This method exhibits good functional group tolerance and a wide range of substrate scope.

Copper(I)-Catalyzed regioselective amination of N -aryl imines using TMSN3 and TBHP: A route to substituted benzimidazoles

Mahesh, Devulapally,Sadhu, Pradeep,Punniyamurthy, Tharmalingam

, p. 1644 - 1650 (2015/02/19)

A novel and efficient copper-catalyzed amination of N-aryl imines is described. This one-pot, multicomponent reaction, in which imine acts as a directing group by chelating to the metal center, affords a potential route for the transformation of the commercial aryl amines, aldehydes, and azides into valuable benzimidazole structural units with wide substrate scope and diversity. The synthetic and mechanistic aspects are presented.

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