64768-20-3 Usage
Description
2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE is a chiral building block that plays a crucial role in the synthetic preparation of saponins and glycosides. It is characterized by the presence of benzyl groups at the 2, 3, 4, and 6 positions, which contribute to its unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Industry:
2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE is used as a chiral building block for the synthesis of saponins and glycosides, which are important compounds in the development of pharmaceuticals. These compounds have various biological activities, such as anti-inflammatory, antifungal, and antiviral properties, making them valuable for the treatment of various diseases and conditions.
Used in Organic Synthesis:
2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE is also used as a versatile intermediate in organic synthesis. Its unique structure allows for various chemical reactions, such as glycosylation, to be performed, enabling the synthesis of a wide range of complex organic molecules with potential applications in various fields, including medicine, agriculture, and materials science.
Used in Research and Development:
2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSE serves as a valuable tool in research and development, particularly in the field of carbohydrate chemistry. Its unique properties and reactivity make it an ideal candidate for studying the structure, function, and interactions of carbohydrates, which can lead to a better understanding of their role in biological systems and the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 64768-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,6 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64768-20:
(7*6)+(6*4)+(5*7)+(4*6)+(3*8)+(2*2)+(1*0)=153
153 % 10 = 3
So 64768-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C34H28O10/c35-30(22-13-5-1-6-14-22)40-21-26-27(42-31(36)23-15-7-2-8-16-23)28(43-32(37)24-17-9-3-10-18-24)29(34(39)41-26)44-33(38)25-19-11-4-12-20-25/h1-20,26-29,34,39H,21H2/t26-,27-,28+,29-,34u/m1/s1
64768-20-3Relevant articles and documents
GLUCOSE-RESPONSIVE INSULIN CONJUGATES
-
Page/Page column 119; 141, (2021/02/05)
Glucose-responsive insulin conjugates that contain one or more trisaccharides are provided. Such insulin conjugates may display a pharmacokinetic (PK) and/or pharmacodynamic (PD) profile that is responsive to the systemic concentrations of a saccharide such as glucose or alpha-methylmannose, even when administered to a subject in need thereof in the absence of an exogenous multivalent saccharide-binding molecule.
Glycosylation with 3,5-Dimethyl-4-(2′-phenylethynylphenyl)phenyl (EPP) Glycosides via a Dearomative Activation Mechanism
Hu, Zhifei,Tang, Yu,Yu, Biao
supporting information, p. 4806 - 4810 (2019/03/26)
A highly effective and versatile glycosylation method is developed, which uses 3,5-dimethyl-4-(2′-phenylethynylphenyl)phenyl (EPP) glycosides as donors and NIS/TMSOTf as promoter and proceeds via an unprecedented dearomative activation mechanism.
2′-Deoxy-2′,2′-difluorothymidine analogues for radiolabeling with fluorine-18 and other biomedical applications
Doepner, Andreas M.,Aboagye, Eric O.,Barrett, Anthony G.M.
supporting information, p. 3293 - 3297 (2015/03/04)
Novel 2′-deoxy-2′,2′-difluorothymidine analogues with potential applications as antiviral, cytotoxic and cancer imaging agents have been synthesized. Introduction of the hydroxymethyl functionality at the 5-position of 2′-deoxy-2′,2′-difluoruridine provided a key intermediate with a suitable synthetic handle for the generation of these nucleoside derivatives.
