178318-63-3 Usage
Molecular structure
A rhamnose sugar molecule extensively modified with acetyl and benzoyl groups.
Solubility
Altered due to the presence of acetyl and benzoyl groups, potentially affecting its solubility in different solvents.
Reactivity
The chemical modifications can change the reactivity of the rhamnose molecule, making it more or less reactive depending on the specific application.
Biological activity
The modified rhamnose molecule may have different biological activities compared to the unmodified rhamnose, which can be useful in studying the interactions and functions of rhamnose-containing molecules in biological systems.
Applications
Can be used as a building block for the synthesis of other complex molecules, as well as in studies of the interactions and functions of rhamnose-containing molecules in biological systems.
Fields of use
Valuable tool for researchers in the fields of chemistry, biochemistry, and pharmaceuticals.
Stereochemistry
The compound has an α-L-rhamnopyranose configuration, which is important for its stereochemical properties and interactions with other molecules.
Functional groups
Contains acetyl and benzoyl functional groups, which contribute to its unique properties and reactivity.
Synthesis
The compound can be synthesized through various chemical reactions, involving the modification of a rhamnose sugar molecule with acetyl and benzoyl groups.
Purity
The purity of the compound is important for its performance in various applications, and it may require purification techniques to remove impurities and byproducts from the synthesis process.
Check Digit Verification of cas no
The CAS Registry Mumber 178318-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,3,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 178318-63:
(8*1)+(7*7)+(6*8)+(5*3)+(4*1)+(3*8)+(2*6)+(1*3)=163
163 % 10 = 3
So 178318-63-3 is a valid CAS Registry Number.
178318-63-3Relevant academic research and scientific papers
Synthetic Cyclic Oligosaccharides - Syntheses and Structural Properties of a Cyclo(1->4)-α-L-rhamnopyranosyl-(1->4)-α-D-mannopyranosyl>trioside and -tetraoside
Ashton, Peter R.,Brown, Christopher L.,Menzer, Stephan,Nepogodiev, Sergey A.,Stoddart, J. Fraser,Williams, David J.
, p. 580 - 591 (2007/10/03)
An efficient polycondensation-cyclization approach to the synthesis of cyclodextrin analogues is demonstrated by the preparation of cyclohexaoside 1 and cyclooctaoside 2.The key intermediate, disaccharide 3, bearing the cyanoethylidene group as a glycosyl
