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1-Benzyl-2',3'-O-isopropylideneinosine is a complex organic compound with the molecular formula C19H23NO4. It is a derivative of inosine, a nucleoside that is a component of RNA. The compound is characterized by the presence of a benzyl group attached to the first carbon of the inosine molecule and an isopropylidene group bridging the 2' and 3' carbons of the ribose sugar moiety. This modification is often used in chemical synthesis to protect the hydroxyl groups of the ribose, which can be crucial for certain reactions. The compound is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or as a research tool in studying the structure and function of nucleic acids.

7026-47-3

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7026-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7026-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7026-47:
(6*7)+(5*0)+(4*2)+(3*6)+(2*4)+(1*7)=83
83 % 10 = 3
So 7026-47-3 is a valid CAS Registry Number.

7026-47-3Relevant academic research and scientific papers

Intramolecular cation-π interactions as the driving force to restrict the conformation of certain nucleosides

Casanova, Elena,Priego, Eva-Maria,Jimeno, Maria-Luisa,Aguado, Leire,Negri, Ana,Gago, Federico,Camarasa, Maria-Jose,Perez, Maria-Jesus

experimental part, p. 1974 - 1981 (2010/05/19)

"Chemical Equation Presented" Despite the well-established importance of intermolecular cation-π interactions in molecular recognition, intramolecular cation-jr interactions have been less studied. Here we describe how the simultaneous presence of an arom

An efficient synthesis of futalosine

Li, Xu,Tanner, Martin E.

scheme or table, p. 6463 - 6465 (2010/12/25)

Futalosine is a naturally occurring nucleoside comprised of an inosine core with a 3-carboxyphenyl methylene ketone functionality replacing the C-5′ hydroxyl. Recent studies have shown that it is a key intermediate in an alternative biosynthetic pathway that generates menaquinone in a variety of bacterial species. Here we report the first synthesis of futalosine in seven steps from inosine in an overall 17% yield. This work will enable further studies on menaquinone biosynthesis in pathogenic bacteria.

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