141120-58-3 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-1-benzyl-2-phenylpiperidin-4-one is used as an intermediate in the synthesis of pharmaceutical drugs due to its unique molecular structure and potential pharmacological properties.
Used in Precursor Compounds:
(R)-1-benzyl-2-phenylpiperidin-4-
one is utilized as a precursor to other chemical compounds, highlighting its versatility and potential for further research and development in the chemical industry.
Used in Psychoactive Substance Research:
(R)-1-benzyl-2-phenylpiperidin-4-one is used in the study of psychoactive substances, as it may exhibit activity in this area. Further research is needed to fully understand its specific effects and mechanisms of action.
Used in Medicinal Chemistry:
(R)-1-benzyl-2-phenylpiperidin-4-one is employed in medicinal chemistry for its potential applications in the development of new drugs and therapies, given its promising pharmacological properties and chiral nature.
Check Digit Verification of cas no
The CAS Registry Mumber 141120-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,2 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141120-58:
(8*1)+(7*4)+(6*1)+(5*1)+(4*2)+(3*0)+(2*5)+(1*8)=73
73 % 10 = 3
So 141120-58-3 is a valid CAS Registry Number.
141120-58-3Relevant academic research and scientific papers
Asymmetric aza-Diels-Alder reaction: Enantio- and diastereoselective reaction of imine mediated by Chiral Lewis acid
Hattori, Kouji,Yamamoto, Hisashi
, p. 1749 - 1760 (2007/10/02)
An efficient asymmetric aza-Diels-Alder reaction using chiral boron mediator is developed. The key to its success is the use of the chiral boron complex prepared in situ from (R)- or (S)- binaphthol and B(OPh)3. The enantiomeric reaction of prochiral imine affords products of up to 90% ee. The double asymmetric induction of chiral imine using α-benzylamine as a chiral auxiliary is achieved with almost complete diastereoselectivity for both aliphatic and aromatic aldimines. This method is applied to the efficient synthesis anabasine and coniine of piperidine alkaloides.
