14227-90-8 Usage
General Description
TRI-O-ACETYL-BETA-L-ARABINOSYLBROMIDE is a chemical compound used primarily in carbohydrate chemistry and related fields. It is a derivative of beta-L-arabinose, a naturally occurring sugar found in plants. The compound is often used as a building block in the synthesis of more complex carbohydrate molecules. TRI-O-ACETYL-BETA-L-ARABINOSYLBROMIDE is known for its ability to selectively protect the primary hydroxyl group of the arabinose sugar, allowing for specific chemical modifications to be made at other sites on the molecule. Its unique properties make it a valuable tool for researchers studying the biological roles and chemical reactivity of carbohydrates. Additionally, it has potential applications in the development of new pharmaceuticals, diagnostics, and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 14227-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14227-90:
(7*1)+(6*4)+(5*2)+(4*2)+(3*7)+(2*9)+(1*0)=88
88 % 10 = 8
So 14227-90-8 is a valid CAS Registry Number.
14227-90-8Relevant articles and documents
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Felton,Freudenberg
, p. 1637,1638 (1935)
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Lewis acid promoted anomerisation of alkyl O- and S-xylo-, arabino- and fucopyranosides
Doyle, Lisa M.,Meany, Fiach B.,Murphy, Paul V.
, p. 85 - 94 (2018/12/05)
Pentopyranoside and 6-deoxyhexopyranosides, such as those from D-xylose, L-arabinose and L-fucose are components of natural products, oligosaccharides or polysaccharides. Lewis acid promoted anomerisation of some of their alkyl O- and S-glycopyranosides i
Synthesis of enantiomerically pure enones (2-benzyloxypyran-3-ones)derived from pentoses
Dada, Lucas,Manzano, Verónica E.,Varela, Oscar
, p. 31 - 40 (2019/05/24)
The useful synthons sugar enones (2-benzyloxypyran-3-ones)derived from pentoses have been prepared starting from 2-acetoxyglycals or benzyl pentopyranosides. The glycals were glycosylated with benzyl alcohol in the presence of a Lewis acid (SnCl4/su