291758-13-9 Usage
Uses
Used in Pharmaceutical Applications:
(R)-1,4-Anhydro-2-O-(2,4-dimethoxybenzoyl)-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-sulfinyl-D-ribitol may be utilized as an active pharmaceutical ingredient or a key intermediate in the synthesis of drugs targeting various medical conditions. Its unique structural features could provide novel mechanisms of action or improved pharmacokinetic properties.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-1,4-Anhydro-2-O-(2,4-dimethoxybenzoyl)-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-sulfinyl-D-ribitol could serve as a valuable building block or precursor for the creation of more complex molecules with specific functions. Its structural diversity and the presence of multiple functional groups make it a promising candidate for further chemical modifications and optimizations.
Used in Materials Science:
(R)-1,4-Anhydro-2-O-(2,4-dimethoxybenzoyl)-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-sulfinyl-D-ribitol's unique structure, including the tetraisopropyldisiloxane-1,3-diyl moiety, may endow it with properties that are beneficial for the development of new materials with specific characteristics, such as improved thermal stability, mechanical strength, or chemical resistance. Further research would be required to explore these potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 291758-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,7,5 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 291758-13:
(8*2)+(7*9)+(6*1)+(5*7)+(4*5)+(3*8)+(2*1)+(1*3)=169
169 % 10 = 9
So 291758-13-9 is a valid CAS Registry Number.
291758-13-9Relevant academic research and scientific papers
Improving RNA interference in mammalian cells by 4′-thio-modified small interfering RNA (siRNA): Effect on siRNA activity and nuclease stability when used in combination with 2′-O-alkyl modifications
Dande, Prasad,Prakash, Thazha P.,Sioufi, Namir,Gaus, Hans,Jarres, Russell,Berdeja, Andreas,Swayze, Eric E.,Griffey, Richard H.,Bhat, Balkrishen
, p. 1624 - 1634 (2007/10/03)
A systematic structure-activity relationship study of 4′-thioribose containing small interfering RNAs (siRNAs) has led to the identification of highly potent and stable antisense constructs. To enable this optimization effort for both in vitro and in vivo
The stereoselective synthesis of 4'-β-thioribonucleosides via the pummerer reaction
Naka, Takashi,Minakawa, Noriaki,Abe, Hiroshi,Kaga, Daisuke,Matsuda, Akira
, p. 7233 - 7243 (2007/10/03)
An efficient stereoselective synthesis of 4'-β-thioribonucleosides 14, 15, 27, and 30 using the Pummerer reaction as the key step is described. The Pummerer reaction of 1,4-anhydro-2-O-(2,4-dimethoxybenzoyl)-3,5-O-(1,1,3,3-tetraisopro pyldisiloxane-1,3-di
