4261-27-2 Usage
Description
2,3-di-O-methyl-D-glucose is a chemical compound derived from glucose, with two methyl groups added to the 2nd and 3rd positions on the carbon ring. This modification changes the chemical properties of glucose, influencing its interactions with other molecules. It serves as a valuable research tool for studying glucose transport and metabolism in cells and holds potential for applications in drug delivery, pharmaceutical development, and therapeutic treatments for various diseases and conditions, although further research is necessary to fully elucidate its biological effects.
Uses
Used in Research Applications:
2,3-di-O-methyl-D-glucose is used as a research tool for studying glucose transport and metabolism in cells, providing insights into the role of glucose in biological systems.
Used in Pharmaceutical Development:
2,3-di-O-methyl-D-glucose is utilized in the development of pharmaceuticals, potentially enhancing drug delivery and targeting specific biological processes.
Used in Drug Delivery Systems:
2,3-di-O-methyl-D-glucose is used as a component in drug delivery systems to improve the efficiency and specificity of drug targeting, potentially leading to more effective treatments.
Used in Therapeutic Applications:
While still under investigation, 2,3-di-O-methyl-D-glucose may have therapeutic uses in treating various diseases and conditions, offering new avenues for medical treatment.
Used in Biotechnology:
2,3-di-O-methyl-D-glucose's unique properties make it a candidate for applications in biotechnology, where it could be employed to manipulate or understand complex biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 4261-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4261-27:
(6*4)+(5*2)+(4*6)+(3*1)+(2*2)+(1*7)=72
72 % 10 = 2
So 4261-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O6/c1-12-7-6(11)5(10)4(3-9)14-8(7)13-2/h4-11H,3H2,1-2H3/t4-,5-,6-,7+,8?/m1/s1
4261-27-2Relevant articles and documents
Mackie,Perlin
, p. 2039,2046 (1966)
Structure characterization of polysaccharide isolated from the fruiting bodies of Tricholoma matsutake
Ding, Xiang,Feng, Su,Cao, Mei,Li, Mao-tao,Tang, Jie,Guo, Chun-xiao,Zhang, Jie,Sun, Qun,Yang, Zhi-rong,Zhao, Jian
experimental part, p. 942 - 947 (2011/12/02)
A novel heteropolysaccharide was isolated from the fruiting bodies of Tricholoma matsutake through DEAE-cellulose column and Sephadex G-100 column. The T. matsutake polysaccharide (TMP-A) had a molecular weight of 8.89 × 104 Da and was mainly composed of 4-D-Glc:4,6-D-Glc:3-D-Gal:T-D-Xyl and with the ratio of 7:1:1:1. The structural features of TMP-A were investigated by a combination of total hydrolysis, methylation analysis, gas chromatography-mass spectrometry (GC-MS), scanning electron microscope (SEM), infrared (IR) spectra, nuclear magnetic resonance (NMR) spectroscopy and dynamical analysis of the atomic force microscope (AFM) studies. The results indicated that TMP-A had a backbone of 1,4-β-glucopyranos which branches at O-6 composed of an (1 → 3)-α-galactopyranose residue and terminated with α-xylopyranose residue. Chain conformation study showed that the polysaccharide took random coil compact conformation.
