959908-09-9 Usage
Uses
Used in Organic Synthesis:
(1R)-7-FLUOROINDANYLAMINE is used as a building block in organic synthesis for the creation of different molecules, including pharmaceuticals and bioactive compounds. Its unique structure and versatility make it a valuable asset in the development of new chemical entities.
Used in Pharmaceutical Research:
(1R)-7-FLUOROINDANYLAMINE is utilized in pharmaceutical research due to its potential biological activity. The presence of a fluorine atom in the molecule can enhance its biological properties, making it a promising candidate for drug development and medicinal chemistry research.
Used in Drug Development:
The fluorine atom in (1R)-7-FLUOROINDANYLAMINE can increase its potential for use in drug development by improving its pharmacokinetic and pharmacodynamic properties. This can lead to the advancement of new therapeutic agents with enhanced efficacy and safety profiles.
Used in Medicinal Chemistry Research:
(1R)-7-FLUOROINDANYLAMINE serves as a valuable tool in medicinal chemistry research, where it can be used to study the structure-activity relationships of various compounds and to develop novel therapeutic agents with improved biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 959908-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,9,0 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 959908-09:
(8*9)+(7*5)+(6*9)+(5*9)+(4*0)+(3*8)+(2*0)+(1*9)=239
239 % 10 = 9
So 959908-09-9 is a valid CAS Registry Number.
959908-09-9Relevant academic research and scientific papers
Asymmetric intramolecular alkylation of chiral aromatic imines via catalytic C-H bond activation
Watzke, Anja,Wilson, Rebecca M.,O'Malley, Steven J.,Bergman, Robert G.,Ellman, Jonathan A.
, p. 2383 - 2389 (2008/03/13)
The asymmetric intramolecular alkylation of chiral aromatic aldimines, in which differentially substituted alkenes are tethered meta to the imine, was investigated. High enantioselectivities were obtained for imines prepared from aminoindane derivatives, which function as directing groups for the rhodium-catalyzed C-H bond activation. Initial demonstration of catalytic asymmetric intramolecular alkylation also was achieved by employing a sterically hindered achiral imine substrate and catalytic amounts of a chiral amine. Georg Thieme Verlag Stuttgart.
