129575-89-9 Usage
Description
4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE, with the CAS number 129575-89-9, is a significant glycoside building block that plays a crucial role in the synthesis of glycans. It is a complex organic compound with a unique structure that allows it to be a valuable component in the creation of various glycan structures.
Uses
Used in Pharmaceutical Industry:
4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE is used as a glycoside building block for the synthesis of glycans, which are essential in the development of various pharmaceutical compounds. The compound's unique structure allows for the creation of diverse glycan structures, which can be utilized in the design and synthesis of new drugs targeting specific biological pathways.
Used in Chemical Research:
In the field of chemical research, 4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE serves as an important compound for studying the properties and interactions of glycosides. Its unique structure provides researchers with valuable insights into the behavior of similar compounds and their potential applications in various industries.
Used in Material Science:
4-METHOXYPHENYL 3,6-DI-O-BENZYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE can also be utilized in material science for the development of novel materials with specific properties. The compound's unique structure and functional groups can be exploited to create materials with tailored characteristics, such as improved biocompatibility or enhanced mechanical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 129575-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129575-89:
(8*1)+(7*2)+(6*9)+(5*5)+(4*7)+(3*5)+(2*8)+(1*9)=169
169 % 10 = 9
So 129575-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C35H33NO8/c1-40-25-16-18-26(19-17-25)43-35-30(36-33(38)27-14-8-9-15-28(27)34(36)39)32(42-21-24-12-6-3-7-13-24)31(37)29(44-35)22-41-20-23-10-4-2-5-11-23/h2-19,29-32,35,37H,20-22H2,1H3/t29-,30-,31-,32-,35-/m1/s1
129575-89-9Relevant articles and documents
Synthesis of glycosyl acceptors by regioselective benzylations of a 2-deoxy-2-phthalimido-D-glucoside
Robina, Inmaculada,Lopez-Barba, Eugenia,Fuentes, Jose
, p. 2847 - 2856 (1996)
The direct regioselective benzylation of p-methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside (1) with benzyl bromide under basic conditions gives 4,6-di-O-benzyl (2a), 4-O-benzyl (3a) and 6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 4a. When
Chemoenzymatic approach for the preparation of asymmetric bi-, tri-, and tetra-antennary N-glycans from a common precursor
Gagarinov, Ivan A.,Li, Tiehai,Tora?o, Javier Sastre,Caval, Tomislav,Srivastava, Apoorva D.,Kruijtzer, John A. W.,Heck, Albert J. R.,Boons, Geert-Jan
, p. 1011 - 1018 (2017/05/16)
Progress in glycoscience is hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate the next generation of microarrays, to develop analytical protocols to determine exact structures of isolated glycans, and to elu
Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals
Zinin, Alexander I.,Malysheva, Nelly N.,Shpirt, Anna M.,Torgov, Vladimir I.,Kononov, Leonid O.
, p. 627 - 630 (2008/03/13)
Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with