518987-75-2 Usage
Description
5-CYANO INDAZOLE-3-CARBOXALDEHYDE is a chemical compound with the molecular formula C10H7N3O, belonging to the indazole family of heterocyclic aromatic organic compounds. Its unique structure, featuring a cyano group and a carboxaldehyde group, renders it a significant precursor for the synthesis of pharmaceuticals, agrochemicals, and dyes. 5-CYANO INDAZOLE-3-CARBOXALDEHYDE's structural properties and reactivity have positioned it as a valuable intermediate in organic synthesis and a promising building block for the development of novel organic compounds.
Uses
Used in Pharmaceutical Industry:
5-CYANO INDAZOLE-3-CARBOXALDEHYDE is used as a key intermediate for the synthesis of potential anti-cancer and anti-inflammatory drugs. Its unique chemical structure allows for the development of new therapeutic agents that can target specific biological pathways and exhibit improved efficacy and safety profiles.
Used in Agrochemical Industry:
5-CYANO INDAZOLE-3-CARBOXALDEHYDE serves as a precursor for the synthesis of agrochemicals, including pesticides and herbicides. Its reactivity and structural properties enable the creation of novel compounds with enhanced pesticidal and herbicidal activities, contributing to more effective and environmentally friendly agricultural practices.
Used in Dye Industry:
5-CYANO INDAZOLE-3-CARBOXALDEHYDE is utilized as a building block for the synthesis of various dyes, particularly those with unique color properties and stability. Its incorporation into dye molecules can lead to the development of new dyes with improved performance characteristics, such as enhanced colorfastness and resistance to fading.
Used in Materials Science:
5-CYANO INDAZOLE-3-CARBOXALDEHYDE is being studied for its potential applications in materials science, where its unique structural properties and reactivity can be harnessed to develop new materials with specific properties. These materials could find use in various fields, such as electronics, optoelectronics, and nanotechnology.
Used in Organic Synthesis:
5-CYANO INDAZOLE-3-CARBOXALDEHYDE is employed as a valuable intermediate in organic synthesis, enabling the creation of a wide range of novel organic compounds with diverse applications. Its versatility and reactivity make it an essential component in the synthesis of complex organic molecules, contributing to advancements in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 518987-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,9,8 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 518987-75:
(8*5)+(7*1)+(6*8)+(5*9)+(4*8)+(3*7)+(2*7)+(1*5)=212
212 % 10 = 2
So 518987-75-2 is a valid CAS Registry Number.
518987-75-2Relevant articles and documents
An optimized procedure for direct access to 1: H -indazole-3-carboxaldehyde derivatives by nitrosation of indoles
Chevalier, Arnaud,Ouahrouch, Abdelaaziz,Arnaud, Alexandre,Gallavardin, Thibault,Franck, Xavier
, p. 13121 - 13128 (2018/04/23)
Indazole derivatives are currently drawing more and more attention in medicinal chemistry as kinase inhibitors. 1H-indazole-3-carboxaldehydes are key intermediates to access to a variety of polyfunctionalized 3-substituted indazoles. We report here a general access to this motif, based on the nitrosation of indoles in a slightly acidic environment. These very mild conditions allow the conversion of both electron-rich and electron-deficient indoles into 1H-indazole-3-carboxaldehydes.
Indazolecarboxamide derivatives, preparation and use thereof as CDK1, CDK2 and CDK4 inhibitors
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Page/Page column 18, (2008/06/13)
Compound corresponding to general formula (I): [image] in which, R1 represents a hydrogen or halogen atom, an NH2, NHR2, NHCOR2, NO2, CN, CH2NH2 and CH2NHR2; or alternatively R1 represents an optionally substituted phenyl or an optionally substituted heteroaromatic group; Ar represents an optionally substituted phenyl group or an optionally substituted heteroaromatic group; n represents 0, 1, 2 or 3; in the form of a base, of an addition salt with an acid, of a hydrate or of a solvate. Application in therapy.
