295779-82-7 Usage
Uses
Used in Organic Synthesis:
6-Fluoro-5-Methoxy-2,3-dihydro-1H-inden-1-one is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for further functionalization and modification, enabling the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
6-Fluoro-5-Methoxy-2,3-dihydro-1H-inden-1-one is used as a starting material or building block in the design and synthesis of new pharmaceutical agents. Its unique chemical properties, such as the presence of a fluorine atom and a methoxy group, can contribute to the development of drugs with improved pharmacokinetic and pharmacodynamic profiles.
Used in Drug Development:
6-Fluoro-5-Methoxy-2,3-dihydro-1H-inden-1-one has potential applications in the development of new drugs due to its unique chemical structure. It can be used as a template for the design of novel therapeutic agents targeting various diseases and conditions. The presence of the fluorine atom and methoxy group can enhance the drug's potency, selectivity, and metabolic stability.
Used in Material Science:
6-Fluoro-5-Methoxy-2,3-dihydro-1H-inden-1-one can also be used in the development of new materials with specific properties. Its unique structure can be incorporated into polymers, coatings, or other materials to impart desired characteristics, such as improved thermal stability, chemical resistance, or optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 295779-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,5,7,7 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 295779-82:
(8*2)+(7*9)+(6*5)+(5*7)+(4*7)+(3*9)+(2*8)+(1*2)=217
217 % 10 = 7
So 295779-82-7 is a valid CAS Registry Number.
295779-82-7Relevant academic research and scientific papers
Transformations of organic molecules with F-TEDA-BF4 in ionic liquid media
Pavlinac, Jasminka,Zupan, Marko,Stavber, Stojan
experimental part, p. 2394 - 2409 (2009/12/03)
The transformations of organic molecules with F-TEDA-BF4 (1) were investigated in the hydrophilic ionic liquid (IL) 1-butyl-3-methyl- imidazolium tetrafluoroborate ([bmim][BF4], 2) and the hydrophobic IL 1-butyl-3-methyl-imidazolium hexafluorophosphate ([bmim][PF6], 3). The range of substrates included alkyl substituted phenols 4a-c, 9, 13, 1,1-diphenylethene (15), alkyl aryl ketones 19-22, aldehydes 23-25 and methoxy-substituted benzene derivatives 26-30. The evaluation of the outcome of reactions performed in IL media in comparison to those of the corresponding reactions in conventional organic solvents revealed that the transformations in IL are less efficient and selective. The effect of the presence of a nucleophile (MeOH, H2O, MeCN) on the course of reaction was also studied.
Solvent directing immediate fluorination of aromatic ketones using 1- fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
Stavber, Stojan,Jereb, Marjan,Zupan, Marko
, p. 1323 - 1324 (2007/10/03)
Reactions of aryl alkyl ketones with 1-fluoro-4-hydroxy1,4- diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Accufluor(TM) NFTh) in methanol result in selective and almost quantitative formation of the corresponding α-fluoroketones, while in acetonitrile exclusive fluorofunctionalisation of the activated aromatic ring take place.
