1027754-32-0 Usage
Uses
Used in Pharmaceutical Industry:
(1R,9R,4'R)-(+)-10,10-dimethyl-4-[4'-phenyl-4',5'-dihydrooxazol-2'-yl]-3-aza-tricyclo[7.1.1.02,7]-undeca-2(7),3,5-triene is used as a potential pharmaceutical agent due to its complex structure and chiral nature, which may offer unique biological activities. The presence of various functional groups could allow it to interact with biological targets in ways that could be harnessed for therapeutic purposes.
Used in Chemical Research:
In the field of chemical research, (1R,9R,4'R)-(+)-10,10-dimethyl-4-[4'-phenyl-4',5'-dihydrooxazol-2'-yl]-3-aza-tricyclo[7.1.1.02,7]-undeca-2(7),3,5-triene serves as a subject of study for understanding the effects of molecular structure on chemical and physical properties. Its unique configuration and functional groups make it an interesting candidate for exploring the principles of stereochemistry and its impact on reactivity.
Used in Material Science:
(1R,9R,4'R)-(+)-10,10-dimethyl-4-[4'-phenyl-4',5'-dihydrooxazol-2'-yl]-3-aza-tricyclo[7.1.1.02,7]-undeca-2(7),3,5-triene may also find applications in material science, where its structural features could be exploited to develop new materials with specific properties. (1R,9R,4'R)-(+)-10,10-dimethyl-4-[4'-phenyl-4',5'-dihydrooxazol-2'-yl]-3-aza-tricyclo[7.1.1.02,7]-undeca-2(7),3,5-triene's potential uses in this field would depend on further investigation into its physical and chemical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 1027754-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,7,5 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1027754-32:
(9*1)+(8*0)+(7*2)+(6*7)+(5*7)+(4*5)+(3*4)+(2*3)+(1*2)=140
140 % 10 = 0
So 1027754-32-0 is a valid CAS Registry Number.
1027754-32-0Relevant academic research and scientific papers
New pinene-derived pyridines as bidentate chiral ligands
Malkov, Andrei V.,Stewart-Liddon, Angus J.P.,Teply, Filip,Kobr, Luká?,Muir, Kenneth W.,Haigh, David,Ko?ovsky, Pavel
, p. 4011 - 4025 (2008/09/20)
A synthesis of new bidentate pyridines 8a-d, 9, and 10 has been developed, starting from triflate 14, readily available from β-pinene 11. A copper complex of the pyridine-oxazoline ligands 8a has been found to catalyze asymmetric allylic oxidation of cyclic olefins 36a-c with good conversion rates and acceptable enantioselectivity (≤67% ee). The imidazolium salt 10 has been identified as a precursor of the corresponding N,N′-unsymmetrical N-heterocyclic carbene ligand, whose complex with palladium catalyzed the intramolecular amide enolate α-arylation leading to oxindole 45 in excellent yield but with low enantioselectivity.
