41926-06-1 Usage
General Description
1-Methyl-1H-indazol-7-ylamine is a chemical compound with the molecular formula C8H9N3. It is a derivative of indazole and belongs to the class of organic compounds known as monoalkylamines. 1-METHYL-1H-INDAZOL-7-YLAMINE is primarily used in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential use in the treatment of certain medical conditions, including cancer and bacterial infections. Overall, 1-methyl-1H-indazol-7-ylamine plays a crucial role in the development and production of a wide range of important chemical and pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 41926-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41926-06:
(7*4)+(6*1)+(5*9)+(4*2)+(3*6)+(2*0)+(1*6)=111
111 % 10 = 1
So 41926-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3/c1-11-8-6(5-10-11)3-2-4-7(8)9/h2-5H,9H2,1H3
41926-06-1Relevant articles and documents
Reduction of nitroindazoles: Preparation of new amino and chloroamino derivatives
Miloudi, Abdellah,El Abed, Douniazed,Boyer, Gerard,Galy, Jean-Pierre
, p. 2595 - 2605 (2008/02/04)
The synthesis of chloroaminoindazoles by the reduction of the nitro group of indazoles using stannous chloride in alcoholic acid solution is reported. Using catalytic hydrogenation with palladium the expected reduction to amino-indazoles occur.{A figure is presented}. Indazole Nitro Reduction Chlorination Aminochloroindazole Heterocycle.
New and efficient synthesis of bi- and trisubstituted indazoles
Bouissane, Latifa,El Kazzouli, Sa?d,Léger, Jean-Michel,Jarry, Christian,Rakib, El Mostapha,Khouili, Mostafa,Guillaumet, Gérald
, p. 8218 - 8225 (2007/10/03)
In this paper, the synthesis of bi- and trisubstituted indazoles was described. 4-Alkoxy-7-aminoprotected-indazole or 7-aminoprotected-indazole derivatives were prepared selectively using SnCl2 in alcohol or SnCl2 in ethyl acetate, r
