1824-88-0 Usage
Description
.alpha.-D-Glucofuranoside, methyl is a methyl derivative of .alpha.-D-Glucofuranoside, a type of sugar molecule commonly used in pharmaceutical and research applications. It serves as a building block for the synthesis of various glycosides, which are crucial components in the development of drugs and other bioactive molecules. This chemical compound has been studied for its potential biological activities, such as modulating cellular processes and its possible use as an anti-inflammatory or anti-cancer agent. Overall, .alpha.-D-Glucofuranoside, methyl plays a significant role in organic chemistry and holds promise for the development of new therapeutics.
Uses
Used in Pharmaceutical Applications:
.alpha.-D-Glucofuranoside, methyl is used as a building block for the synthesis of various glycosides, which are essential in the development of drugs and other bioactive molecules. Its role in creating these compounds contributes to the advancement of pharmaceutical research and drug development.
Used in Research Applications:
In the field of research, .alpha.-D-Glucofuranoside, methyl is utilized for studying its potential biological activities, including its role in modulating cellular processes. This research can lead to a better understanding of the compound's properties and its potential applications in various scientific areas.
Used in Organic Chemistry:
.alpha.-D-Glucofuranoside, methyl plays an important role in organic chemistry, particularly in the synthesis of complex sugar molecules and their derivatives. Its unique structure and properties make it a valuable compound for exploring new chemical reactions and developing novel chemical methodologies.
Used in Anti-inflammatory Applications:
.alpha.-D-Glucofuranoside, methyl has been studied for its potential use as an anti-inflammatory agent. If its anti-inflammatory properties are confirmed, it could be used in the development of new treatments for various inflammatory conditions.
Used in Anti-cancer Applications:
.alpha.-D-Glucofuranoside, methyl has also been investigated for its potential as an anti-cancer agent. If its anti-cancer properties are proven, .alpha.-D-Glucofuranoside, methyl could be used in the development of new therapeutic strategies for cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 1824-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1824-88:
(6*1)+(5*8)+(4*2)+(3*4)+(2*8)+(1*8)=90
90 % 10 = 0
So 1824-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O6/c1-12-7-5(11)4(10)6(13-7)3(9)2-8/h3-11H,2H2,1H3/t3-,4-,5-,6-,7+/m1/s1
1824-88-0Relevant articles and documents
Facile synthesis of methyl α- and β-d-[6-3H]galactofuranosides from d-galacturonic acid. Substrates for the detection of galactofuranosidases
Bordoni, Andrea,Lima, Carlos,Marino, Karina,de Lederkremer, Rosa M.,Marino, Carla
, p. 1863 - 1869 (2008)
Galactofuranose metabolism is a good target for the development of novel chemotherapeutic agents for the treatment of some microbial infections. A simple procedure for the synthesis of methyl (methyl α,β-d-galactopyranosid)uronate followed by NaB3H4 reduction gave a straightforward access to radiolabeled substrates for galactofuranosidases.
A Systematic Study of Metal Triflates in Catalytic Transformations of Glucose in Water and Methanol: Identifying the Interplay of Br?nsted and Lewis Acidity
Bodachivskyi, Iurii,Kuzhiumparambil, Unnikrishnan,Williams, D. Bradley G.
, (2019/04/25)
The specific type of acidity associated with the given metal trifloromethanesulfonates (Br?nsted or Lewis acidity) dramatically influences the course of reactions, and it is possible to select for disaccharides, fructose, methyl glucosides, or methyl levulinate. Glucose is transformed into a range of value-added molecules in water and methanol under the action of acidic metal triflates as catalysts, including their analogous Br?nsted acid-assisted or Br?nsted base-modified systems. A systematic study is presented of a range of metal triflates in methanol and water, pinning down the preferred conditions to select for each product.
Reaction of D-fructose, D-glucose and inulin with alcohols in the presence of iodine; a novel glycosidation procedure
Verhart, Cor G.J.,Fransen, Carel T.M.,Zwanenburg, Binne,Chittenden, Gordon J.F.
, p. 133 - 139 (2007/10/03)
An efficient procedure for the glycosidation of D-fructose and D-glucose catalyzed by iodine is described. The reaction yields mainly alkyl glycofuranosides. Treatment of inulin under similar conditions leads to inter-glycosidic bond cleavage and to formation of alkyl D-fructofuranosides. The reaction conditions are particularly mild and relatively selective.
