75785-12-5 Usage
Uses
Used in Pharmaceutical Industry:
7-Methyl-5-nitro-1H-indazole is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable building block in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 7-methyl-5-nitro-1H-indazole is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the creation of compounds that can effectively control pests and weeds, contributing to improved crop yields and agricultural productivity.
Used in Research Applications:
7-Methyl-5-nitro-1H-indazole also serves as a valuable research tool in various scientific fields. Its unique chemical properties make it suitable for use in the study of chemical reactions, synthesis processes, and the development of new materials and compounds. Researchers can leverage its characteristics to explore novel applications and enhance existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 75785-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,8 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75785-12:
(7*7)+(6*5)+(5*7)+(4*8)+(3*5)+(2*1)+(1*2)=165
165 % 10 = 5
So 75785-12-5 is a valid CAS Registry Number.
75785-12-5Relevant academic research and scientific papers
Buchwald reaction as the key step for the synthesis of metabolically more stable analogs of amodiaquine
Le Fur, Nicolas,Hochart, Guillaume,Larchanché, Paul-Emmanuel,Melnyk, Patricia
, p. 3052 - 3057 (2011/07/08)
Amodiaquine is one of the most active anti-malarial 4-aminoquinoline but its metabolization is believed to generate hepatotoxic derivatives. Previously, we described new analogs of amodiaquine and amopyroquine, in which hydroxyl group was replaced by vari
Anisotropy Effects of Conjugated Cyclic Systems, IV. 1H-NMR Spectra of Mesityl-Substituted 2,6-Dimethylbenzene Derivatives
Brotzeller, Uwe,Nyitrai, Jozsef,Musso, Hans
, p. 3610 - 3620 (2007/10/02)
The effect of very different substituents X on the chemical shift differences Δδ of the o- and p-methyl group 1H NMR signals of 4'-X-substituted 2,2',4,6,6'-pentamethylbiphenyl derivatives is +/- 0.045 ppm only.In comparison with X = H (0.47 ppm) electron attracting substitutents like X = N2+ increase Δδ values up to 0.53, X = CN and NO2 up to 0.52 ppm; electron releasing groups X = OH, NH2 reduce Δδ down to 0.45 and OCH3 to 0.44 ppm.Even in the 2-mesitylsubstituted 1,3,5,-trimethyltropylium ion (2) Δδ rises only up to 0.54 ppm.
