186790-80-7 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3S)-2,3-Dihydroxy-4-isopropoxy-γ-butyrolactone Cyclohexyl Ketal is used as an intermediate in the preparation of Mannostatin derivatives. Mannostatin derivatives are known for their potential applications in the development of novel pharmaceuticals, particularly those targeting various diseases and conditions.
Used in Chemical Synthesis:
As a complex organic molecule, (2R,3S)-2,3-Dihydroxy-4-isopropoxy-γ-butyrolactone Cyclohexyl Ketal can be utilized as a key intermediate in the synthesis of other complex organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the development of new molecules with specific properties and applications.
Used in Research and Development:
Due to its unique structure and potential for further modification, (2R,3S)-2,3-Dihydroxy-4-isopropoxy-γ-butyrolactone Cyclohexyl Ketal can be employed in research and development settings. It can be used to explore new reaction pathways, study the effects of structural modifications on chemical properties, and investigate potential applications in various fields, such as materials science, pharmaceuticals, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 186790-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,7,9 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 186790-80:
(8*1)+(7*8)+(6*6)+(5*7)+(4*9)+(3*0)+(2*8)+(1*0)=187
187 % 10 = 7
So 186790-80-7 is a valid CAS Registry Number.
186790-80-7Relevant academic research and scientific papers
Reinvestigation of the synthesis of (2R,3R) 2,3-(cyclohexylidenedioxy)-4-cyclopentenone as possible building block for the synthesis of carbocyclic nucleosides
Marien,Esmans,Lemiere,Dommisse
, p. 205 - 224 (2007/10/03)
An in depth study of the four-steps synthesis of (2R,3R) 2,3-(cyclohexylidenedioxy)-4-cyclopentenone (5) from D-ribonolactone (1) is described. From these experiments we must conclude that the overall yield reported in the literature (65%) is overestimated. All compounds have been throughly investigated by 1H- and 13C-NMR spectroscopy.
