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D,L-epi-inosose is a rare ketose sugar, a type of monosaccharide, that is structurally similar to inositol. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is found in both D and L forms. D,L-epi-inosose is synthesized through the isomerization of D,L-inosose, which is derived from the hydrolysis of inositol. D,L-epi-inosose has gained interest in the scientific community due to its potential applications in various fields, such as pharmaceuticals and biotechnology. It exhibits unique properties, including the ability to inhibit certain enzymes and its potential role in the regulation of cellular processes. Despite its promise, more research is needed to fully understand its biological activities and potential therapeutic uses.

488-65-3

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488-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488-65-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 488-65:
(5*4)+(4*8)+(3*8)+(2*6)+(1*5)=93
93 % 10 = 3
So 488-65-3 is a valid CAS Registry Number.

488-65-3Relevant academic research and scientific papers

Protecting group directed stereoselective reduction of an epi-inosose: Efficient synthesis of epi-inositol

Patil, Madhuri T.,Krishnaswamy, Shobhana,Sarmah, Manash P.,Shashidhar, Mysore S.

, p. 3756 - 3758 (2011)

A facile and high yielding synthesis of epi-inositol via stereoselective reduction of a pentaprotected epi-inosose is reported. Extent of stereoselectivity during the hydride reduction appears to depend on the ability of the substrate to complex with metal ions in the reducing agent.

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