488-64-2 Usage
General Description
Inosose is a chemical compound that belongs to the class of carbohydrate derivatives known as inositol glycosides. It is a cyclic sugar derivative that is commonly found in trace amounts in certain plants and microorganisms. Inosose has been found to have potential pharmaceutical and biotechnological applications due to its unique chemical structure and properties. It has been studied for its potential use as a drug carrier or stabilizer in pharmaceutical formulations, as well as its role in the production of natural products and biofuels. In addition, inosose has shown promise as a potential therapeutic agent for the treatment of various diseases, including cancer and neurodegenerative disorders. Its wide range of potential applications makes inosose an interesting and valuable chemical compound for further research and development.
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.
Stereochemical recognition of doubly functional aminotransferase in 2-deoxystreptamine biosynthesis
Yokoyama, Kenichi,Kudo, Fumitaka,Kuwahara, Mieko,Inomata, Kousuke,Tamegai, Hideyuki,Eguchi, Tadashi,Kakinuma, Katsumi
, p. 5869 - 5874 (2007/10/03)
The doubly functional aminotransferase BtrS in the 2-deoxystreptamine (DOS) biosynthesis, in which two transaminations are involved, was characterized by a genetic as well as a chemical approach with the heterologously expressed enzyme. The gene disruptio
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)
-
