80887-27-0 Usage
Description
2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl Azide is a complex organic compound with a unique structure that features a benzylidene group and azide functionality. It is characterized by its potential reactivity and versatility in chemical synthesis and molecular modeling.
Uses
Used in Chemical Synthesis:
2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl Azide is used as a key intermediate in the synthesis of complex organic molecules, particularly in the preparation of N,N'',N''''-triacetylchitotriose pseudosugar analogs. Its unique structure allows for the formation of various derivatives with potential applications in different fields.
Used in Molecular Modeling:
2-ACETAMIDO-3-O-BENZYL-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is also utilized in molecular modeling conformational analysis, providing insights into the structural properties and interactions of complex organic molecules. Its unique features make it a valuable tool for understanding the behavior of similar compounds in biological systems.
Used in Green Chemistry:
2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl Azide is employed in the visible-light-mediated regioselective green preparation of triazoles via iridium-catalyzed photocycloaddition of azides with alkynes. This method represents an environmentally friendly approach to the synthesis of triazoles, which are important building blocks in various chemical and pharmaceutical applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl Azide is used as a precursor for the development of novel drug candidates. Its unique structure and reactivity make it a promising starting material for the synthesis of bioactive compounds with potential therapeutic applications.
Used in Materials Science:
In materials science, 2-Acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl Azide can be used as a building block for the design and synthesis of new materials with specific properties. Its versatility in chemical reactions allows for the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for energy storage and conversion.
Check Digit Verification of cas no
The CAS Registry Mumber 80887-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,8 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80887-27:
(7*8)+(6*0)+(5*8)+(4*8)+(3*7)+(2*2)+(1*7)=160
160 % 10 = 0
So 80887-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H24N4O5/c1-14(27)24-18-20(28-12-15-8-4-2-5-9-15)19-17(30-21(18)25-26-23)13-29-22(31-19)16-10-6-3-7-11-16/h2-11,17-22H,12-13H2,1H3,(H,24,27)/t17-,18-,19-,20-,21-,22-/m1/s1
80887-27-0Relevant articles and documents
The Synthesis of Antigenic Glycopeptides, 2-Acetamido-N-(β-L-aspartyl)-2-deoxy-4-O-β-(D-galactopyranosyl)-β-D-glucopyranosylamine. (N-Acetyllactosaminyl-L-asparagine)
Shaban, Mohammed Abd El-Monem,Jeanloz, Roger W.
, p. 3570 - 3576 (2007/10/02)
The title compound, serving as intermediate in the chemical and biochemical synthesis of glycopeptides and as a reference substance in the structure elucidation of glycoproteins, was synthesized. 2-Acetamido-4-O-allyl-3,6-di-O-benzyl-2-deoxy-β-D-glucopyra
