712352-04-0 Usage
Uses
Used in Organic Chemistry Research:
S-N-Methyl-N-[(1S)-1-phenylethyl]-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-aMine is utilized as a subject of study in organic chemistry for its unique molecular structure and potential applications in the synthesis of novel compounds.
Used in Materials Science:
In the field of materials science, S-N-Methyl-N-[(1S)-1-phenylethyl]-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-aMine is employed to explore its potential in developing new materials with specific properties due to its complex chemical composition and structure.
Check Digit Verification of cas no
The CAS Registry Mumber 712352-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,2,3,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 712352-04:
(8*7)+(7*1)+(6*2)+(5*3)+(4*5)+(3*2)+(2*0)+(1*4)=120
120 % 10 = 0
So 712352-04-0 is a valid CAS Registry Number.
712352-04-0Relevant academic research and scientific papers
Efficient, selective, and green: Catalyst tuning for highly enatioselective reactions of ethylene
Smith, Craig R.,Rajanbabu
supporting information; experimental part, p. 1657 - 1659 (2009/04/10)
Fine tuning of the biaryl and amino moieties of Feringa's phosphoramidite ligands yields structurally simpler, yet more efficient and selective, ligands for asymmetric hydrovinylation of vinylarenes and acylic 1,3-dienes. The enantioselectivities and yields observed in the formation of the 3-arylbutenes are among the highest for all asymmetric catalytic processes reported to date for the synthesis of intermediates for the widely used antiinflammatory 2-arylpropionic acids including naproxen, ibuprofen, fenoprofen, and flurbiprofen.
