905809-90-7 Usage
Uses
Used in Pharmaceutical Industry:
(7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(3-FLUOROPHENYL)METHANONE is used as a potential therapeutic agent for various medical conditions due to its potential biological activities. (7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(3-FLUOROPHENYL)METHANONE's unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Drug Discovery and Development:
In the field of drug discovery and development, (7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(3-FLUOROPHENYL)METHANONE serves as a valuable chemical scaffold for the design and synthesis of novel compounds with potential therapeutic applications. Its unique structure and properties can be exploited to create new drugs with improved efficacy, selectivity, and safety profiles.
Used in Research and Development:
(7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(3-FLUOROPHENYL)METHANONE is also used as a research tool to study the structure-activity relationships of benzodioxin derivatives and their potential applications in various biological processes. This knowledge can be applied to the development of new drugs and therapies for a wide range of diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 905809-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,8,0 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 905809-90:
(8*9)+(7*0)+(6*5)+(5*8)+(4*0)+(3*9)+(2*9)+(1*0)=187
187 % 10 = 7
So 905809-90-7 is a valid CAS Registry Number.
905809-90-7Relevant academic research and scientific papers
A new effective route for the synthesis of substituted 2H-indazoles
Mochalov,Khasanov,Trofimova,Fedotov,Zefirov
experimental part, p. 1208 - 1217 (2010/06/12)
A two-stage synthesis of 2H-indazoles has been established, based on consecutive reactions of reduction of 2-alkyl-, 2-cyclopropyl-, and 2-arylcarbonylazobenzenes to phenylazo-substituted benzyl alcohols and intramolecular heterocyclization of the reducti
