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Benzenamine, N-[(3,4-dichlorophenyl)methylene]-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63462-40-8

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63462-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63462-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63462-40:
(7*6)+(6*3)+(5*4)+(4*6)+(3*2)+(2*4)+(1*0)=118
118 % 10 = 8
So 63462-40-8 is a valid CAS Registry Number.

63462-40-8Relevant academic research and scientific papers

Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino Acids

Ji, Peng,Zhang, Yueteng,Wei, Yongyi,Huang, He,Hu, Wenbo,Mariano, Patrick A.,Wang, Wei

, p. 3086 - 3092 (2019)

An approach for efficient synthesis of C-glycosyl amino acids is described. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylations using both armed and disarmed pentose and hexose derivatives.

One-pot sequential multicomponent reaction between: In situ generated aldimines and succinaldehyde: Facile synthesis of substituted pyrrole-3-carbaldehydes and applications towards medicinally important fused heterocycles

Singh, Anoop,Mir, Nisar A.,Choudhary, Sachin,Singh, Deepika,Sharma, Preetika,Kant, Rajni,Kumar, Indresh

, p. 15448 - 15458 (2018/05/03)

An efficient sequential multi-component method for the synthesis of N-Arylpyrrole-3-carbaldehydes has been developed. This reaction involved a proline-catalyzed direct Mannich reaction-cyclization sequence between succinaldehyde and in situ generated Ar/H

Enantioselective synthesis of 1,2,5,6-tetrahydropyridines (THPs): Via proline-catalyzed direct Mannich-cyclization/domino oxidation-reduction sequence: Application for medicinally important N-heterocycles

Ramaraju, Panduga,Mir, Nisar A.,Singh, Deepika,Kumar, Indresh

, p. 60422 - 60432 (2016/07/11)

An enantioselective multi-component synthesis of 1,2,5,6-tetrahydropyridines (THPs) has been developed through a one-pot domino-process. This transformation proceeds through proline-catalyzed direct Mannich reaction-cyclization of glutaraldehyde with in s

One-pot synthesis and fluorescence properties of 2-arylquinolines

Sueki, Shunsuke,Okamoto, Chiharu,Shimizu, Isao,Seto, Keisuke,Furukawa, Yukio

supporting information; experimental part, p. 385 - 390 (2010/07/09)

The one-pot synthesis of 2-arylquinoline with arylamines, arylaldehyde, and 1,1-diethoxyethane were studied using a catalytic amount ytterbium triflate. Various 2-arylquinolines showed fluorescence properties and the fluorescence was quenched by introduci

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