708-40-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(6-Chloro-1H-indazol-1-yl)ethanone is used as a synthetic intermediate for the development of new pharmaceuticals. Its reactivity allows for the creation of diverse drug molecules, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1-(6-Chloro-1H-indazol-1-yl)ethanone is utilized as an intermediate in the synthesis of agricultural chemicals. Its role in formulating effective and novel agrochemicals is pivotal for enhancing crop protection and yield.
Used in Research and Development:
1-(6-Chloro-1H-indazol-1-yl)ethanone also serves as a research chemical, facilitating the exploration and development of innovative pharmaceuticals and chemical processes. Its application in research is instrumental for scientific discovery and the improvement of existing chemical methodologies.
Safety Note:
Given the potentially hazardous nature of 1-(6-Chloro-1H-indazol-1-yl)ethanone, it is imperative to adhere to proper safety precautions and handling procedures when working with 1-(6-Chloro-1H-indazol-1-yl)ethanone. This ensures the well-being of individuals in the laboratory and the integrity of the chemical processes involved.
Check Digit Verification of cas no
The CAS Registry Mumber 708-40-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 708-40:
(5*7)+(4*0)+(3*8)+(2*4)+(1*0)=67
67 % 10 = 7
So 708-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2O/c1-6(13)12-9-4-8(10)3-2-7(9)5-11-12/h2-5H,1H3
708-40-7Relevant academic research and scientific papers
Aromatic Diazonium Salts, X. - A One-Pot Procedure for the Jacobson Synthesis of Indazole
Ruechardt, Christoph,Hassmann, Volker
, p. 908 - 927 (2007/10/02)
Procedures are described for a one-pot synthesis of 1H-indazole and substituted indazoles 3 in good yield (Table 1) from o-toluidines 2, alkyl nitrite or nitrous oxides, potassium acetate, and acetic anhydride in benzene.The spectroscopic properties of substituted indazoles (Tables 2-4) are discussed. - 4-Phenylcinnoline (18) is prepared by the same procedure from o-(α-methylenebenzyl)aniline.