3616-19-1 Usage
Description
ALPHA-D-CELLOBIOSE OCTAACETATE is a chemical compound derived from D-(+)-Cellobiose, a disaccharide composed of two glucose units. It is characterized by the presence of eight acetate groups attached to its hydroxyl groups, which significantly alters its properties and reactivity compared to the parent compound. This modification makes it a versatile intermediate in organic synthesis and a valuable building block for the preparation of various biologically active molecules.
Uses
Used in Pharmaceutical Industry:
ALPHA-D-CELLOBIOSE OCTAACETATE is used as a key intermediate in the synthesis of glycosphingolipid analogs, which are important for studying the interactions between these lipids and HIV-1 recombinant Gp120. This application is crucial for understanding the mechanisms of viral infection and developing potential therapeutic agents against HIV.
Used in Organic Synthesis:
As a versatile building block, ALPHA-D-CELLOBIOSE OCTAACETATE is used in the preparation of various complex organic molecules, including pharmaceuticals, agrochemicals, and other bioactive compounds. Its reactivity and functional group compatibility make it an attractive starting material for the development of novel chemical entities with potential applications in various industries.
Used in Research and Development:
Due to its unique structure and properties, ALPHA-D-CELLOBIOSE OCTAACETATE is employed in research and development settings to explore its potential applications in various fields, such as drug discovery, material science, and chemical biology. Its use in these areas can lead to the development of innovative products and technologies that can benefit society.
Check Digit Verification of cas no
The CAS Registry Mumber 3616-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3616-19:
(6*3)+(5*6)+(4*1)+(3*6)+(2*1)+(1*9)=81
81 % 10 = 1
So 3616-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C28H38O19/c1-11(29)37-9-19-21(39-13(3)31)23(40-14(4)32)26(43-17(7)35)28(46-19)47-22-20(10-38-12(2)30)45-27(44-18(8)36)25(42-16(6)34)24(22)41-15(5)33/h19-28H,9-10H2,1-8H3/t19?,20?,21-,22-,23-,24-,25?,26?,27+,28+/m1/s1
3616-19-1Relevant articles and documents
Synthesis of aryl glycosides as vir gene inducers of Agrobacterium tumefaciens
Delay,Cizeau,Delmotte
, p. 179 - 188 (2007/10/02)
Aryl β-glycopyranosides have been synthesized by coupling syringaldehyde (3-methoxyvanillin) with L-fucose, D-galactose, and maltose; acetosyringone (4-hydroxy-3,5-dimethoxyacetophenone) with L-fucose and maltose; acetovanillone (4-hydroxy-3-methoxyacetophenone) with L-fucose; and syringic acid (4-hydroxy-3,5-dimethoxybenzoic acid) with D-galactose. The procedure using peracetylated glycosyl halides and sodium phenolates in aqueous acetone afforded the acetylated β-glycosides, which were deacetylated. Aryl β-glycopyranosides have been synthesized by coupling syringaldehyde (3-methoxyvanillin) with L-fucose, D-galactose, and maltose; acetosyringone (4-hydroxy-3,5-dimethoxyacetophenone) with L-fucose and maltose; acetovanillone (4-hydroxy-3-methoxyacetophenone) with L-fucose; and syringic acid (4-hydroxy-3,5-dimethoxybenzoic acid) with D-galactose. The procedure using peracetylated glycosyl halides and sodium phenolates in aqueous acetone afforded the acetylated β-glycosides, which were deacetylated.
