488-64-2 Usage
Description
Inosose is a carbohydrate derivative belonging to the class of inositol glycosides. It is a cyclic sugar derivative that can be found in trace amounts in certain plants and microorganisms. Due to its unique chemical structure and properties, inosose has potential pharmaceutical and biotechnological applications.
Uses
Used in Pharmaceutical Formulations:
Inosose is used as a drug carrier or stabilizer for enhancing the efficacy and stability of pharmaceutical formulations.
Used in Production of Natural Products and Biofuels:
Inosose serves as a key component in the production of natural products and biofuels, contributing to the development of sustainable energy sources and eco-friendly products.
Used in Therapeutic Applications:
Inosose is used as a potential therapeutic agent for the treatment of various diseases, including cancer and neurodegenerative disorders, due to its promising medicinal properties.
Used in Research and Development:
Inosose is utilized in research and development for further exploration of its potential applications and to unlock new possibilities in the fields of medicine, biotechnology, and energy.
Check Digit Verification of cas no
The CAS Registry Mumber 488-64-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 488-64:
(5*4)+(4*8)+(3*8)+(2*6)+(1*4)=92
92 % 10 = 2
So 488-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-5,7-11H/t1?,2-,3+,4+,5-
488-64-2Relevant articles and documents
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.
supporting information; experimental part, p. 3756 - 3758 (2011/08/06)
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.
Stereoselective oxidation of protected inositol derivatives catalyzed by inositol dehydrogenase from Bacillus subtilis
Daniellou, Richard,Phenix, Christopher P.,Tam, Pui Hang,Laliberte, Michael C.,Palmer, David R. J.
, p. 401 - 403 (2007/10/03)
Inositol dehydrogenase (EC 1.1.1.18) from Bacillus subtilis is shown to have a nonpolar cavity adjacent to the active site, allowing racemic protected inositol derivatives such as 4-O-benzyl-myo-inositol to be recognized with very high apparent stereoselectivity.
Synthesis of 1,2,3,4-tetrahydroxybenzene from D-glucose: Exploiting myo- inositol as a precursor to aromatic chemicals [11]
Hansen, Chad A.,Dean, Amy B.,Draths,Frost
, p. 3799 - 3800 (2007/10/03)
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