1824-88-0

Basic information

• Product Name: .alpha.-D-Glucofuranoside, methyl
• Synonyms: .alpha.-D-Glucofuranoside, methyl
• CAS NO: 1824-88-0
• Molecular Formula: C₇H₁₄O₆
• Molecular Weight: 0
• Mol File: 1824-88-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 444.8°Cat760mmHg
• Flash Point: 222.8°C
• Appearance: /
• Density: 1.47g/cm³
• Vapor Pressure: 8.81E-10mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: .alpha.-D-Glucofuranoside, methyl(CAS DataBase Reference)
• NIST Chemistry Reference: .alpha.-D-Glucofuranoside, methyl(1824-88-0)
• EPA Substance Registry System: .alpha.-D-Glucofuranoside, methyl(1824-88-0)

Safety Data

• Hazardous Substances Data: 1824-88-0(Hazardous Substances Data)

Usage

General Description

".alpha.-D-Glucofuranoside, methyl" is a chemical compound that is a methyl derivative of .alpha.-D-Glucofuranoside. It is a type of sugar molecule that is commonly used in pharmaceutical and research applications. .alpha.-D-Glucofuranoside, methyl is often utilized as a building block for the synthesis of various glycosides, which are important components in the development of drugs and other bioactive molecules. Additionally, .alpha.-D-Glucofuranoside, methyl has been studied for its potential biological activities, including its role in modulating various cellular processes and its potential use as an anti-inflammatory or anti-cancer agent. Overall, this chemical compound plays an important role in the field of organic chemistry and has potential applications in the development of new therapeutics.

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

Upstream product

• 67-56-1 methanol 
• 2280-44-6 D-Glucose 
• 50-99-7 D-glucose 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 109129-09-1 (1Ξ)-O¹-methyl-1-(4-nitro-anilino)-D-glucitol 
• 109129-15-9 (1Ξ)-1-(4-chloro-anilino)-O¹-methyl-D-glucitol 

Relevant articles and documents

Facile synthesis of methyl α- and β-d-[6-3H]galactofuranosides from d-galacturonic acid. Substrates for the detection of galactofuranosidases

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

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

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.