1824-89-1 Usage
Description
.beta.-D-Glucofuranoside, methyl is a chemical compound that consists of a methyl group attached to a .beta.-D-Glucofuranoside molecule. It is a type of glycoside, which is a molecule formed from a sugar and another compound, in this case, a methyl group. .beta.-D-Glucofuranoside, methyl is commonly used in chemical synthesis, particularly in the production of pharmaceuticals and other organic compounds. It also serves as a building block in the creation of more complex molecules and may have potential medicinal applications, although further research is needed to fully understand its pharmaceutical uses.
Uses
Used in Pharmaceutical Industry:
.beta.-D-Glucofuranoside, methyl is used as a key compound in the synthesis of various pharmaceuticals. Its unique structure allows it to be a valuable building block for the development of new drugs, potentially leading to the creation of innovative treatments for various medical conditions.
Used in Organic Chemistry:
In the field of organic chemistry, .beta.-D-Glucofuranoside, methyl is used as a starting material for the synthesis of more complex organic molecules. Its versatile structure makes it a valuable tool for researchers and chemists working on the development of new compounds with specific properties and applications.
Used in Research and Development:
.beta.-D-Glucofuranoside, methyl may also be used in research and development settings to explore its potential medicinal applications. Further studies are needed to understand its full potential in the pharmaceutical industry, but its unique structure and properties make it a promising candidate for future drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 1824-89-1 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 1824-89:
(6*1)+(5*8)+(4*2)+(3*4)+(2*8)+(1*9)=91
91 % 10 = 1
So 1824-89-1 is a valid CAS Registry Number.
1824-89-1Relevant articles and documents
Kinetically Controlled Fischer Glycosidation under Flow Conditions: A New Method for Preparing Furanosides
Masui, Seiji,Manabe, Yoshiyuki,Hirao, Kohtaro,Shimoyama, Atsushi,Fukuyama, Takahide,Ryu, Ilhyong,Fukase, Koichi
supporting information, p. 397 - 400 (2019/02/26)
Kinetically controlled Fischer glycosidation was achieved under flow conditions. β-Hydroxy-substituted sulfonic acid functionalized silica (HO-SAS) was used as an acid catalyst. This reaction directly converted aldohexoses into kinetically favored furanosides to enable the practical synthesis of furanosides. After optimization of the reaction temperature and residence time, glucofuranosides, galactofuranosides, and mannofuranosides were synthesized in good yields.
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 (2008/12/22)
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.
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.
