75829-66-2 Usage
Description
(-)-(4,6-O-BENZYLIDENE)PHENYL-BETA-D-GLUCOPYRANOSIDE is a glucose derivative glycoside compound characterized by the presence of a benzylidene moiety and a phenyl group. It is formed by the combination of a sugar molecule, glucose, with another group, and has potential applications in medicinal and pharmaceutical fields due to its glucose-based structure and the presence of benzylidene and phenyl groups.
Used in Pharmaceutical Industry:
(-)-(4,6-O-BENZYLIDENE)PHENYL-BETA-D-GLUCOPYRANOSIDE is used as a potential compound for exhibiting biological activities in medicinal and pharmaceutical fields, due to its glucose-based structure and the presence of benzylidene and phenyl groups.
Used in Chemical Synthesis:
(-)-(4,6-O-BENZYLIDENE)PHENYL-BETA-D-GLUCOPYRANOSIDE is used as a reagent or building block in chemical synthesis for the development of other compounds with specific properties.
Further research and testing are necessary to fully understand and utilize the properties and potential applications of (-)-(4,6-O-benzylidene)phenyl-β-D-glucopyranoside.
Check Digit Verification of cas no
The CAS Registry Mumber 75829-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,2 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75829-66:
(7*7)+(6*5)+(5*8)+(4*2)+(3*9)+(2*6)+(1*6)=172
172 % 10 = 2
So 75829-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O6/c20-15-16(21)19(23-13-9-5-2-6-10-13)24-14-11-22-18(25-17(14)15)12-7-3-1-4-8-12/h1-10,14-21H,11H2/t14-,15-,16-,17-,18?,19-/m1/s1
75829-66-2Relevant articles and documents
Chiral recognition of amino-acid esters by a glucose-derived macrocyclic receptor
Dominique, Pit,Schnurr, Martin,Lewandowski, Bartosz
supporting information, p. 3476 - 3479 (2021/04/12)
We report a glucose-based crown ether capable of chiral recognition of a wide range of amino-acid methyl esters in aqueous environments. The enantioselectivities towards amino-acids with extended hydrophobic side chains displayed by the glucose-derived ma
Novel cyclic phosphate-linked oligosaccharides (CyPLOSs) covalently immobilized on solid supports for potential cation scavenging
D'Onofrio, Jennifer,Coppola, Cinzia,Fabio, Giovanni Di,De Napoli, Lorenzo,Montesarchio, Daniela
, p. 3849 - 3858 (2008/02/13)
For potential cation scavenging both from water and from organic solvents, here we propose a synthetic procedure for functionalization of a Tentagel solid support with novel cyclic phosphate-linked oligosaccharide (CyPLOS) analogues. To establish the feas
Novel amphiphilic cyclic oligosaccharides: Synthesis and self-aggregation properties
Coppola, Cinzia,Saggiomo, Vittorio,Di Fabio, Giovanni,De Napoli, Lorenzo,Montesarchio, Daniela
, p. 9679 - 9689 (2008/03/27)
(Chemical Equation Presented) Novel amphiphilic cyclic disaccharide analogues, in which the saccharide units are connected through stable phosphodiester linkages (CyPLOS, Cyclic Phosphate-Linked Oligosaccharides) and decorated with long lipophilic tentacl