53958-20-6 Usage
Description
1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate is a white crystalline solid that is a derivative of a-D-mannopyranose, a monosaccharide. It is characterized by the presence of three acetyl groups at the 1, 4, and 6 positions and a carbonate group at the 2 and 3 positions. 1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate is utilized in various organic synthesis processes due to its unique structural features.
Uses
Used in Organic Synthesis:
1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate is used as an intermediate in organic synthesis for the preparation of various complex molecules, particularly in the field of carbohydrate chemistry. Its unique structure allows for selective functionalization and modification, making it a valuable building block for the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate is used as a key compound in the synthesis of -mannosides, which are important in the development of drugs targeting specific biological receptors. These -mannosides can be used to create glycoconjugates, which have potential applications in the treatment of various diseases, including cancer and infectious diseases.
Used in Material Science:
In the field of material science, 1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate can be used as a component in the development of novel materials with specific properties. Its ability to form complexes with other molecules can be exploited to create materials with tailored characteristics, such as improved biocompatibility or enhanced mechanical properties.
Used in Research and Development:
1,4,6-Tri-O-acetyl-a-D-mannopyranose 2,3-Carbonate is also used as a research tool in academic and industrial laboratories. Its unique structure and reactivity make it an interesting compound for studying various chemical reactions and exploring new synthetic routes. This can lead to the discovery of new compounds with potential applications in various industries, including pharmaceuticals, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 53958-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,5 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53958-20:
(7*5)+(6*3)+(5*9)+(4*5)+(3*8)+(2*2)+(1*0)=146
146 % 10 = 6
So 53958-20-6 is a valid CAS Registry Number.
53958-20-6Relevant articles and documents
PRACTICAL SYNTHESIS OF O-β-D-MANNOPYRANOSYL-, O-α-D-MANNOPYRANOSYL-, AND O-β-D-GLUCOPYRANOSYL-(1->4)-O-α-L-RHAMNOPYRANOSYL-(1->3)-D-GALACTOSES
Betaneli, Vitali I.,Ovchinnikov, Michael V.,Backinowsky, Leon V.,Kochetkov, Nikolay K.
, p. 211 - 224 (2007/10/02)
The Koenigs-Knorr glycosylation of 4,6-O-ethylidene-1,2-O-isopropylidene-3-O-(2,3-O-isopropylidene-α-L-rhamnopyranosyl)-α-D-galactopyranose (3) by 4,6-di-O-acetyl-2,3-O-carbonyl-α-D-mannopyranosyl bromide (10), as well as Helferich glycosylations of 3 by tetra-O-acetyl-α-D-mannopyranosyl and -α-D-glucopyranosyl bromides, proceeded smoothly to give high yields of trisaccharide derivatives (12, 16, and 17).An efficient procedure for the transformation of 12, 16, and 17 into the α-deca-acetates of the respective trisaccharides has been developed.Zemplen deacetylation then afforded the title trisaccharides in yields of 53, 52, and 62percent respectively, from 3.A new route to 1,4,6-tri-O-acetyl-2,3-O-carbonyl-α-D-mannopyranose is suggested.
