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(3R,6S,8S,8aR)-8-ethyl-6-methyl-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

601488-95-3

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601488-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 601488-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,1,4,8 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 601488-95:
(8*6)+(7*0)+(6*1)+(5*4)+(4*8)+(3*8)+(2*9)+(1*5)=153
153 % 10 = 3
So 601488-95-3 is a valid CAS Registry Number.

601488-95-3Relevant academic research and scientific papers

Alkylation of phenylglycinol-derived oxazolopiperidone lactams. Enantioselective synthesis of β-substituted piperidines

Amat, Mercedes,Escolano, Carmen,Lozano, Oscar,Gomez-Esque, Arantxa,Griera, Rosa,Molins, Elies,Bosch, Joan

, p. 3804 - 3815 (2007/10/03)

The stereochemical outcome of the alkylation of a variety of phenylglycinol-derived oxazolopiperidone lactams is studied. The influence of the configuration of the C-8a stereocenter and the effect of the substituents at the C-8 and C-8a positions on the s

Enantioselective synthesis of cis- and trans-3,5-disubstituted piperidines. Synthesis of 20S- and 20R-dihydrocleavamine

Amat, Mercedes,Escolano, Carmen,Lozano, Oscar,Llor, Nuria,Bosch, Joan

, p. 3139 - 3142 (2007/10/03)

(Matrix presented) Diastereoselective alkylation at the carbonyl α-position of chiral nonracemic lactams 2 and 3, the former prepared by cyclocondensation of (R)-phenylglycinol with a racemic γ-substituted δ-oxoester in a process that involves a dynamic k

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