17773-22-7 Usage
General Description
2,5-Anhydro-3,4-dideoxy-2-thiohexaric acid is a complex chemical compound with potential applications in the fields of medicine and biochemistry. It is a sulfur-containing derivative of the sugar molecule, and it possesses unique structural and functional properties. 2,5-Anhydro-3,4-dideoxy-2-thiohexaric acid has been studied for its potential use as a medication in the treatment of various diseases, including cancer and diabetes. Its ability to target specific cellular pathways and its potential to modify enzyme activity make it a promising candidate for further research and development. Additionally, its structural similarity to naturally occurring sugars suggests that it may have potential as a carbohydrate-based drug or therapeutic agent. However, further research and clinical trials are needed to fully understand the potential of this compound in medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17773-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17773-22:
(7*1)+(6*7)+(5*7)+(4*7)+(3*3)+(2*2)+(1*2)=127
127 % 10 = 7
So 17773-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O4S/c7-5(8)3-1-2-4(11-3)6(9)10/h3-4H,1-2H2,(H,7,8)(H,9,10)
17773-22-7Relevant articles and documents
Explorations into the potential of chiral sulfonium reagents to effect asymmetric halonium additions to isolated alkenes
Brucks, Alexandria P.,Treitler, Daniel S.,Liu, Shu-An,Snyder, Scott A.
, p. 1886 - 1898 (2013/07/26)
While methods for the racemic dihalogenation and halohydroxylation of alkenes have been known for decades, enantioselective variants of these processes remain elusive. Initial attempts were made to overcome this long-standing challenge by exploring the potential of chiral, crystalline, sulfur-derived halonium reagents to accomplish the asymmetric dichlorination and iodohydroxylation of 1,2-dihydronaphthalene. Asymmetric dichlorination of this substrate was achieved in 57% yield and 14% enantiomeric excess (ee), but asymmetric iodohydroxylation was much more successful, giving 67% yield and 63% ee. Thorough studies were made of these processes, including investigation of various chiral sulfide derivatives, their substrate scopes, and the reaction conditions. Georg Thieme Verlag Stuttgart · New York.
