145761-32-6 Usage
Description
(5R,6S)-benzyl 3-(diMethoxyphosphoryl)-2-oxo-5,6-diphenylMorpholine-4-carboxylate is a morpholine derivative with a molecular formula of C26H27NO7P. It features a benzyl group at the 5R position and a diMethoxyphosphoryl group at the 3 position of the morpholine ring. Additionally, it has a 2-oxo-5,6-diphenyl group and a carboxylate group attached to the morpholine ring. This unique structural composition may offer potential applications in pharmaceuticals or organic synthesis.
Uses
Used in Pharmaceutical Industry:
(5R,6S)-benzyl 3-(diMethoxyphosphoryl)-2-oxo-5,6-diphenylMorpholine-4-carboxylate is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure may allow it to interact with biological targets, offering possible applications in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (5R,6S)-benzyl 3-(diMethoxyphosphoryl)-2-oxo-5,6-diphenylMorpholine-4-carboxylate can be utilized as a synthetic intermediate or building block for the creation of more complex molecules. Its distinct functional groups may facilitate the synthesis of various organic compounds with specific properties.
Further research and development are required to fully understand the properties and potential uses of (5R,6S)-benzyl 3-(diMethoxyphosphoryl)-2-oxo-5,6-diphenylMorpholine-4-carboxylate, as its current applications are based on its structural features and potential in pharmaceuticals and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 145761-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,6 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145761-32:
(8*1)+(7*4)+(6*5)+(5*7)+(4*6)+(3*1)+(2*3)+(1*2)=136
136 % 10 = 6
So 145761-32-6 is a valid CAS Registry Number.
145761-32-6Relevant articles and documents
Asymmetric synthesis of S-(-)-cucurbitine
Williams,Fegley
, p. 6755 - 6758 (2007/10/02)
The asymmetric synthesis of (S)-(-)-cucurbitine in greater than 98% ee is described. The key step of the synthesis involves 1,3-dipolar cycloaddition of azomethine ylide (1) to α,β-dehydrolactone (3) to give pyrrolidine (6) as a single diastereomer.
