4261-27-2 Usage
General Description
2,3-di-O-methyl-D-glucose is a chemical compound that consists of a glucose molecule with two methyl groups added to the 2 and 3 positions on the carbon ring. This modification alters the chemical properties of glucose and can affect its interactions with other molecules. 2,3-di-O-methyl-D-glucose is commonly used as a research tool to study glucose transport and metabolism in cells, and it has also been investigated for potential applications in drug delivery and pharmaceutical development. Additionally, this compound may have potential therapeutic uses in treating various diseases and conditions, although further research is needed to fully understand its biological effects. Overall, 2,3-di-O-methyl-D-glucose is a valuable tool for studying the role of glucose in biological systems and has potential applications in medicine and biotechnology.
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.
