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1,2,4,5,6-penta-O-acetyl-sn-myo-inositol is a chemical compound derived from myo-inositol, a naturally occurring sugar alcohol. In 1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myo-inositol, five hydroxyl groups of myo-inositol are acetylated, meaning they are each bonded to an acetyl group (CH3CO-). The numbering of the hydroxyl groups indicates their positions on the inositol ring: the 1st, 2nd, 4th, 5th, and 6th positions. This modification significantly alters the physical and chemical properties of the parent compound, potentially affecting its solubility, reactivity, and biological activity. The acetylated form may be used in various applications, such as in pharmaceuticals or as a chemical intermediate.

5517-47-5

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5517-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5517-47-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,1 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5517-47:
(6*5)+(5*5)+(4*1)+(3*7)+(2*4)+(1*7)=95
95 % 10 = 5
So 5517-47-5 is a valid CAS Registry Number.

5517-47-5Relevant academic research and scientific papers

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (Part 2): Via nonsymmetrical conduritol B derivatives

Podeschwa, Michael A. L.,Plettenburg, Oliver,Altenbach, Hans-Josef

, p. 3116 - 3127 (2007/10/03)

A practical route is described for the preparation of myo-inositol phosphates. Optically pure compounds can be prepared, in both forms, from p-benzoquinone by enzymatic resolution of a diacetoxyconduritol key intermediate. Monosubstituted inositol derivat

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