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(2R,3R)-3-(Adenin-9-yl)-2-O-benzyl-2-nonanol is a complex organic compound with a molecular formula of C23H31N5O3. It is a chiral molecule, meaning it has two enantiomers due to the presence of two chiral centers (2R,3R). The compound features an adenine moiety, which is a purine base found in DNA and RNA, attached to a nonanol chain with a benzyl group at the 2-O position. This structure suggests potential applications in medicinal chemistry, particularly in the development of nucleoside analogs or as a building block for more complex molecules. The compound's specific properties, such as solubility, stability, and reactivity, would depend on the context of its intended use and the surrounding chemical environment.

81408-46-0

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81408-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81408-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,0 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81408-46:
(7*8)+(6*1)+(5*4)+(4*0)+(3*8)+(2*4)+(1*6)=120
120 % 10 = 0
So 81408-46-0 is a valid CAS Registry Number.

81408-46-0Downstream Products

81408-46-0Relevant academic research and scientific papers

Synthesis of Inhibitors of Adenosine Deaminase. A Total Synthesis of erythro-3-(Adenin-9-yl)-2-nonanol and Its Isomers from Chiral Precursors

Baker, David C.,Hawkins, L. D.

, p. 2179 - 2184 (2007/10/02)

The synthesis of both isomers of EHNA2 ("erythrohydroxynonyladenine") from D- and L-rhamnose is described.The key intermediates, (R)- and (S)-2-(benzyloxy)propanal, derived respectively from 5-O-benzyl-D- and -L-rhamnitol, were each condensed w

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