100959-52-2 Usage
Uses
Used in Pharmaceutical Industry:
7-AMINO-4-CHLORO INDAZOLE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and anti-cancer properties. Its unique structure allows for the development of new drugs that can target specific biological pathways, offering novel treatment options for a range of diseases.
Used in Organic Synthesis:
7-AMINO-4-CHLORO INDAZOLE is used as a reagent in organic synthesis to create complex organic molecules. Its versatile chemical structure enables the formation of a wide array of compounds with diverse applications, including the development of new materials, dyes, and other specialty chemicals.
Used in Research and Development:
7-AMINO-4-CHLORO INDAZOLE is utilized as a research compound in the exploration of new chemical reactions and the discovery of novel synthetic routes. Its unique properties make it an attractive candidate for studying the reactivity and selectivity of various chemical transformations, contributing to the advancement of synthetic chemistry and the development of new methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 100959-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,5 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100959-52:
(8*1)+(7*0)+(6*0)+(5*9)+(4*5)+(3*9)+(2*5)+(1*2)=112
112 % 10 = 2
So 100959-52-2 is a valid CAS Registry Number.
100959-52-2Relevant academic research and scientific papers
Research in 7-aminoindazole series: Synthesis of new halo-7H-4-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-6-ones and 5H-9-halo-6-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-4-ones
Rakib,Benchidmi,Essassi,El Bouadili,Ibn Mansour,Bellan,Lopez,Lamande
, p. 339 - 345 (2007/10/03)
A new class of 7-aminohaloindazoles has been synthesized. Reactivity of the amino groups of these bicyclic systems has been investigated. The halogenated pyrazolo-1,5-benzodiazepinones have been synthesized by the condensation of 7-aminoindazoles with ethyl acetoacetate.
