293751-01-6 Usage
General Description
3-O-Benzyl-4-C-(methanesulfonyloxymethyl)-5-O-methanesulfonyl-1,2-O-isopropylidene-α-D-ribofuranose is a complex chemical compound with several functional groups attached to a ribofuranose sugar molecule. The benzyl group, methanesulfonyl groups, and isopropylidene group all contribute to its overall structure and reactivity. 3-O-Benzyl4-C-(methanesulfonyloxymethyl)-5-O-methanesulfonyl-1,2-O-isopropylidene-a-D-ribofuranose is often used in organic synthesis as a protecting group for the sugar moiety, allowing for selective manipulation of other functional groups in a molecule. It is an important tool in carbohydrate chemistry for the construction of complex oligosaccharides and glycoconjugates. 3-O-Benzyl4-C-(methanesulfonyloxymethyl)-5-O-methanesulfonyl-1,2-O-isopropylidene-a-D-ribofuranose also has potential applications in the pharmaceutical industry for the development of carbohydrate-based drugs and therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 293751-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,7,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 293751-01:
(8*2)+(7*9)+(6*3)+(5*7)+(4*5)+(3*1)+(2*0)+(1*1)=156
156 % 10 = 6
So 293751-01-6 is a valid CAS Registry Number.
293751-01-6Relevant articles and documents
NOVEL PROCESS FOR MAKING ALLOFURANOSE FROM GLUCOFURANOSE
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, (2019/12/15)
The present invention relates to the manufacture of allofuranose from glucofuranose as defined in the description and in the claim. Allofuranos is an intermediate in the manufacture of oligonucleotides which can be used as a medicament.
Chemoenzymatic convergent synthesis of 2'-o,4'-c-methyleneribonucleosides
Sharma, Vivek K.,Kumar, Manish,Olsen, Carl E.,Prasad, Ashok K.
supporting information, p. 6336 - 6341 (2014/07/21)
Novozyme-435-catalyzed efficient regioselective acetylation of one of the two diastereotopic hydroxymethyl functions in 3-O-benzyl-4-C-hydroxymethyl-1,2- O-isopropylidene-α-d-ribofuranose has been achieved. The enzymatic methodology has been successfully
IMPROVED SYNTHESIS OF ?2.2.1|BICYCLO NUCLEOSIDES
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Page/Page column 10; 34, (2008/06/13)
A synthesis of [2.2.1]bicyclo nucleosides which is shorter and provides higher overall yields proceeds via the key intermediate of the general formula III, wherein R4 and R5 are, for instance, sulfonates and R7 is, for instance, a halogen or an acetate. F