6623-68-3 Usage
Description
(PLUS-MINUS)-EPI-INOSOSE-2 is a chemical compound that belongs to the class of inositol-related compounds. It is an epimeric form of inosose, a type of carbohydrate with several possible stereoisomers. This chemical has potential applications in various fields such as chemistry, biochemistry, and pharmaceuticals due to its unique structural and functional properties. Its properties and reactivity make it a subject of interest for researchers and scientists for further study and potential utilization. Additionally, its epimeric nature adds to its potential versatility and utility in various chemical and biochemical processes.
Uses
Used in Chemical Industry:
(PLUS-MINUS)-EPI-INOSOSE-2 is used as a building block for the synthesis of various complex organic compounds, taking advantage of its unique structural properties and reactivity.
Used in Biochemical Research:
(PLUS-MINUS)-EPI-INOSOSE-2 is used as a research tool for studying the structure and function of inositol-related compounds, as well as their interactions with other biomolecules.
Used in Pharmaceutical Development:
(PLUS-MINUS)-EPI-INOSOSE-2 is used as a potential therapeutic agent in the development of new drugs, leveraging its unique properties and reactivity to target specific biological pathways or processes.
Used in Drug Delivery Systems:
(PLUS-MINUS)-EPI-INOSOSE-2 can be employed as a component in the design of drug delivery systems, potentially enhancing the delivery, bioavailability, and therapeutic outcomes of associated pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 6623-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6623-68:
(6*6)+(5*6)+(4*2)+(3*3)+(2*6)+(1*8)=103
103 % 10 = 3
So 6623-68-3 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
6623-68-3Relevant 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.
