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2-allyl-6-nitro-2H-indazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

501918-63-4

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501918-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501918-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 501918-63:
(8*5)+(7*0)+(6*1)+(5*9)+(4*1)+(3*8)+(2*6)+(1*3)=134
134 % 10 = 4
So 501918-63-4 is a valid CAS Registry Number.

501918-63-4Downstream Products

501918-63-4Relevant academic research and scientific papers

Regioselective synthesis of 2H-indazoles through Ga/Al- and Al-mediated direct alkylation reactions of indazoles

Lin, Mei-Huey,Liu, Han-Jun,Lin, Wei-Cheng,Kuo, Chung-Kai,Chuang, Tsung-Hsun

, p. 11376 - 11381 (2015)

A procedure has been developed for the regioselective, high yielding synthesis of 2H-indazoles that involves direct alkylation of indazoles with various allyl and benzyl bromides, and α-bromocarbonyl compounds.

One-pot synthesis of new 6-pyrrolyl-N-alkyl-indazoles from reductive coupling of N-alkyl-6-nitroindazoles and 2,5-hexadione

El Ghozlani, Mohamed,Chicha, Hakima,Abbassi, Najat,Chigr, Mohamed,El Ammari, Lahcen,Saadi, Mohamed,Spinelli, Domenico,Rakib, El Mostapha

supporting information, p. 113 - 117 (2015/12/23)

One-pot synthesis of 6-pyrrolyl-N-alkyl-indazoles by the reductive coupling of N-alkyl-6-nitroindazoles and 2,5-hexadione was investigated in the presence of different reducing agents (SnCl2/AcOH and In/AcOH in THF). Indazoles 5a-h and 6a-h wer

Alkylation and reduction of N-alkyl-4-nitroindazoles with anhydrous SnCl2 in ethanol: Synthesis of novel 7-ethoxy-N-alkylindazole derivatives

Abbassi, Najat,Rakib, El Mostapha,Hannioui, Abdellah,Alaoui, Mdaghri,Benchidmi, Mohamed,Essassi, El Mokhtar,Geffkenc, Detlef

experimental part, p. 891 - 900 (2011/05/12)

New series of indazoles substituted at the N-1 and N-2 positions and their 7-ethoxy derivatives have been synthesis starting from alkylation of 4-nitroindazole and reduction of alkyl-nitro-derivatives with anhydrous SnCl2 in ethanol. The structures of the

Selective synthesis of 1 -functionalized-alkyl-1H-indazoles

Hunt, Kevin W.,Moreno, David A.,Suiter, Nicole,Clark, Christopher T.,Kim, Ganghyeok

scheme or table, p. 5054 - 5057 (2009/12/28)

An efficient method for the selective "N1" alkylation of indazoles is described. Use of a-halo esters, lactones, ketones, amides, and bromoacetonitrile provides good to excellent yield of the desired N1 products.

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