890936-71-7 Usage
Uses
Used in Pharmaceutical Industry:
(3S)-1-benzyl-6-oxopiperidine-3-carboxylic acid is used as a drug precursor for the development of new pharmaceuticals, due to its potential as a building block in the synthesis of various compounds.
Used in Agrochemical Industry:
(3S)-1-benzyl-6-oxopiperidine-3-carboxylic acid is used as an intermediate in the synthesis of agrochemicals, contributing to the development of new products for agricultural applications.
Used in Medicinal Chemistry:
(3S)-1-benzyl-6-oxopiperidine-3-carboxylic acid is used as a research compound for exploring its potential in medicinal chemistry, where it may contribute to the discovery of new therapeutic agents.
Used in Organic Synthesis:
(3S)-1-benzyl-6-oxopiperidine-3-carboxylic acid is used as a synthetic building block for the creation of novel organic compounds, potentially leading to advancements in various chemical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 890936-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,9,3 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 890936-71:
(8*8)+(7*9)+(6*0)+(5*9)+(4*3)+(3*6)+(2*7)+(1*1)=217
217 % 10 = 7
So 890936-71-7 is a valid CAS Registry Number.
890936-71-7Relevant academic research and scientific papers
Asymmetric Reduction of Lactam-Based β-Aminoacrylates. Synthesis of Heterocyclic β2-Amino Acids
Campello, Hugo Rego,Parker, Jeremy,Perry, Matthew,Ryberg, Per,Gallagher, Timothy
supporting information, p. 4124 - 4127 (2016/08/30)
The ability to affect asymmetric reduction of heterocyclic β-aminoacrylates 1 (n = 1-3) has been assessed with pyrrolidine and piperidone variants generating the corresponding N-heterocyclic β2-amino acids 3b and 5b with high enantioselectivity
A flexible strategy for the synthesis of tri- and tetracyclic lupin alkaloids: Synthesis of (+)-cytisine, (±)-anagyrine, and (±)-thermopsine
Gray, Diane,Gallagher, Timothy
, p. 2419 - 2423 (2007/10/03)
(Chemical Equation Presented) Looping the lupin: A general synthetic strategy for the construction of the lupin alkaloids has been defined and involves sequential formation of the N1-C10 and C6-C7 bonds, which are common to compounds of this class of natu
