25348-62-3 Usage
Uses
Used in Pharmaceutical Industry:
3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE is used as a key intermediate in the synthesis of Conduritol B epoxide, a compound that has been extensively studied for its potential applications in the treatment of cancer, particularly pancreatic cancer. The compound acts as an inhibitor of glucose metabolism, specifically targeting the enzyme aldose reductase, which is involved in the development and progression of cancer cells.
Used in Organic Synthesis:
3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE is also used as a versatile building block in the synthesis of various other organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure allows for a wide range of functional group transformations, making it a valuable tool for chemists in the development of new molecules with diverse applications.
Used in Research and Development:
As a white solid with distinct chemical properties, 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL-1,2-THIOCARBONATE is utilized in research and development laboratories for the exploration of new synthetic routes, the development of novel chemical reactions, and the investigation of its potential applications in various fields, such as materials science, drug discovery, and chemical biology.
Check Digit Verification of cas no
The CAS Registry Mumber 25348-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25348-62:
(7*2)+(6*5)+(5*3)+(4*4)+(3*8)+(2*6)+(1*2)=113
113 % 10 = 3
So 25348-62-3 is a valid CAS Registry Number.
25348-62-3Relevant academic research and scientific papers
SYNTHESIS OF BRANCHED-CHAIN CYCLITOLS USING A PALLADIUM(0)-CATALYZED ALLYLIC COUPLING REACTION
Barton, Derek H. R.,Dalko, Peter,Gero, Stephan D.
, p. 2471 - 2474 (2007/10/02)
A carbanion derived from Meldrum's acid was used in a palladium(0)-catalysed allylic substitution reaction to prepare stereospecifically branched-chain cyclitols from the symmetrical 1,2,3,4-tetraacetoxycyclohex-5-ene (4).
