112168-22-6 Usage
Uses
Used in Organic Synthesis:
[3aS-(3aa,4a,5b,6aa)]-4-[[[(tert-Butyl)dimethylsilyl]oxy]methyl]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexahydro-2(1H)-pentalenone is used as a synthetic intermediate for the development of complex organic molecules, leveraging its protective groups for alcohols to facilitate selective reactions and protect specific functional groups during synthesis.
Used in Medicinal Chemistry:
In the pharmaceutical industry, [3aS-(3aa,4a,5b,6aa)]-4-[[[(tert-Butyl)dimethylsilyl]oxy]methyl]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexahydro-2(1H)-pentalenone may be used as a lead compound for the discovery of new drugs, given its unique structure and potential bioactivity. Its complex nature could offer novel interactions with biological targets, leading to the development of innovative therapeutic agents.
Used in Chemical Research:
[3aS-(3aa,4a,5b,6aa)]-4-[[[(tert-Butyl)dimethylsilyl]oxy]methyl]-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexahydro-2(1H)-pentalenone serves as a subject of study in chemical research to explore its reactivity, properties, and potential applications in various chemical processes, including the development of new synthetic methods and the understanding of its behavior in different chemical environments.
Check Digit Verification of cas no
The CAS Registry Mumber 112168-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,6 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112168-22:
(8*1)+(7*1)+(6*2)+(5*1)+(4*6)+(3*8)+(2*2)+(1*2)=86
86 % 10 = 6
So 112168-22-6 is a valid CAS Registry Number.
112168-22-6Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF ILOPROST
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, (2019/11/12)
The present invention relates to a process for the preparation of iloprost of formula I through new intermediates, isolation of iloprost of formula I in solid form, as well as preparation of the 16(S)-iloprost and 16(R)-iloprost isomers of formulae (S)-I and (R)-I and isolation of iloprost of formula I and 16(S)-iloprost of formula (S)-I in solid, crystalline form.
