444019-07-2 Usage
Sugar derivative
It is a modified version of a sugar molecule, specifically a ribose derivative.
Acetyl groups
The molecule has two acetyl groups (-COCH3) attached to the hydroxyl groups at the 1st and 2nd carbon positions.
Benzoyl group
A benzoyl group (-COPh) is attached to the hydroxyl group at the 5th carbon position.
3-Deoxy
The molecule lacks an oxygen atom at the 3rd carbon position, making it a deoxy sugar.
3-C-methyl
A methyl group (-CH3) is attached to the 3rd carbon position, making it a methylated sugar.
D-ribofuranose
The core structure is a ribose sugar in a furanose ring form.
Organic synthesis
It can be used as a building block for the synthesis of other organic compounds due to its complex structure and multiple functional groups.
Medicinal chemistry research
Its unique structure and potential biological activity make it valuable for research in the development of new pharmaceuticals.
Potential applications
Further research may reveal its applications in various fields, such as pharmaceuticals, materials science, and other industries.
These properties and specific content provide a comprehensive understanding of 1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-C-methyl-D-ribofuranose and its potential uses in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 444019-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,0,1 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 444019-07:
(8*4)+(7*4)+(6*4)+(5*0)+(4*1)+(3*9)+(2*0)+(1*7)=122
122 % 10 = 2
So 444019-07-2 is a valid CAS Registry Number.
444019-07-2Relevant articles and documents
Revisited 3′-deoxy-3′-C-methyl-β-D-ribonucleoside series
Aljarah, Mohamed,Couturier, Sarah,Gosselin, Gilles,Mathe, Christophe,Perigaud, Christian
, p. 1125 - 1128 (2008/09/17)
The synthesis of some 3′-deoxy-3′-C-methylnucleoside analogues bearing naturally occuring nucleic acid bases was achieved from the preparation of a suitable peracylated 3-deoxy-3-C-methyl sugar using a stereoselective pathway. In addition, examples of chemical modifications at the 2′ position are presented. Copyright Taylor & Francis Group, LLC.
