1824-93-7 Usage
Description
Beta-D-Galactofuranoside, methyl is a chemical compound that belongs to the class of glycosides. It is a methyl derivative of beta-D-galactofuranose, which is a sugar molecule. .beta.-D-Galactofuranoside, methyl plays a significant role in biochemical and pharmaceutical research due to its unique properties and potential applications.
Uses
Used in Enzymatic Assays:
Beta-D-Galactofuranoside, methyl is used as a substrate in enzymatic assays for studying the activity of galactofuranosidases. These enzymes are responsible for hydrolyzing glycosidic bonds in galactofuranose-containing compounds, which are crucial for understanding the biological functions and interactions of these molecules.
Used in Metabolism and Biosynthesis Studies:
.beta.-D-Galactofuranoside, methyl is also utilized in the study of the metabolism and biosynthesis of galactofuranose-containing molecules. These molecules are essential components of the cell wall of some microorganisms, making them a significant area of research for understanding microbial biology and developing potential therapeutic strategies.
Used in Pharmaceutical Research:
Beta-D-Galactofuranoside, methyl has potential applications in the development of therapeutic agents targeting galactofuranose-containing compounds. This includes the development of antifungal and antimicrobial drugs, which could be beneficial in treating various infections and diseases caused by microorganisms with galactofuranose-containing cell walls.
Used in Biochemical Research:
In addition to its pharmaceutical applications, beta-D-Galactofuranoside, methyl is also important in biochemical research. It helps researchers understand the structure, function, and interactions of glycosides and other related compounds, contributing to the broader understanding of biochemistry and molecular biology.
Check Digit Verification of cas no
The CAS Registry Mumber 1824-93-7 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, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1824-93:
(6*1)+(5*8)+(4*2)+(3*4)+(2*9)+(1*3)=87
87 % 10 = 7
So 1824-93-7 is a valid CAS Registry Number.
1824-93-7Relevant articles and documents
Methyl glycosides via Fischer glycosylation: translation from batch microwave to continuous flow processing
Aronow, Jonas,Stanetty, Christian,Baxendale, Ian R.,Mihovilovic, Marko D.
, p. 11 - 19 (2018/11/27)
Abstract: A continuous flow procedure for the synthesis of methyl glycosides (Fischer glycosylation) of various monosaccharides using a heterogenous catalyst has been developed. In-depth analysis of the isomeric composition was undertaken and high consistency with corresponding results observed under microwave heating was obtained. Even in cases where addition of water was needed to achieve homogeneity—a prerequisite for the flow experiments—no detrimental effect on the conversion was found. The scalability was demonstrated on a model case (mannose) and as part of the target-oriented synthesis of d-glycero-d-manno heptose, both performed on multigram scale.
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.
A NEW, FACILE METHOD FOR CLEAVAGE OF ACETALS AND DITHIOACETALS IN CARBOHYDRATE DERIVATIVES
Szarek, Walter A.,Zamojski, Aleksander,Tiwari, Kamal N.,Ison, Edward R.
, p. 3827 - 3830 (2007/10/02)
Treatment of carbohydrate acetals and dithioacetals with a dilute solution of iodine in methanol provides a simple, convenient, and high-yielding process for cleavage of the acetal functions.