677702-62-4 Usage
Uses
Used in Organic Synthesis:
4-Bromo-8-nitroisoquinoline is used as a key intermediate in the synthesis of various biologically active compounds due to its unique structural properties and reactivity. It facilitates the creation of a wide range of chemical reactions, contributing to the development of novel organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Bromo-8-nitroisoquinoline is utilized as a starting material for the development of new drugs and pharmaceuticals. Its structural properties and reactivity allow for the exploration of its potential therapeutic applications, making it a promising candidate for drug discovery and design.
Used in Drug Development:
4-Bromo-8-nitroisoquinoline is employed as a building block in the development of innovative drugs, leveraging its chemical stability and diverse reactivity to create new pharmaceutical agents. Its potential applications in drug development highlight its importance in advancing the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 677702-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 677702-62:
(8*6)+(7*7)+(6*7)+(5*7)+(4*0)+(3*2)+(2*6)+(1*2)=194
194 % 10 = 4
So 677702-62-4 is a valid CAS Registry Number.
677702-62-4Relevant academic research and scientific papers
Indazolecarboxamide derivatives, preparation and use thereof as CDK1, CDK2 and CDK4 inhibitors
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Page/Page column 20; 22, (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.