85906-16-7 Usage
Uses
Used in Pharmaceutical Applications:
2,6-anhydro-1-O-[(4-methylphenyl)sulfonyl]hexitol is used as a potential therapeutic agent for its ability to interact with biological targets, which may lead to the development of new drugs or treatments.
Used in Material Science Applications:
In the field of material science, 2,6-anhydro-1-O-[(4-methylphenyl)sulfonyl]hexitol is used as a component in the development of new materials, leveraging its unique physical properties to create innovative products with enhanced characteristics.
Used in Research and Development:
2,6-anhydro-1-O-[(4-methylphenyl)sulfonyl]hexitol is utilized as a subject of study in research settings, where its synthesis and characterization are explored to understand its potential uses in diverse fields and to advance scientific knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 85906-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85906-16:
(7*8)+(6*5)+(5*9)+(4*0)+(3*6)+(2*1)+(1*6)=157
157 % 10 = 7
So 85906-16-7 is a valid CAS Registry Number.
85906-16-7Relevant academic research and scientific papers
Dansyl C-glucoside as a novel agent against endotoxic shock
La Ferla, Barbara,Spinosa, Valerio,D'Orazio, Giuseppe,Palazzo, Marco,Balsari, Andrea,Foppoli, Anastasia A.,Rumio, Cristiano,Nicotra, Francesco
, p. 1677 - 1680 (2011/12/15)
Come dansyl with me! A small library of naphthyl gluco derivatives was synthesised from methyl α-D-glucopyranoside without protection/ deprotection steps. One library member, dansyl C-glucoside 5, showed an extraordinary anti-inflammatory activity, protecting 100□% of mice from sepsis at a dose of 25 μg□kg-1.
SYNTHESIS OF SOME DERIVATIVES OF 6-AMINO-1,5-ANHYDRO-6-DEOXY-D-GLUCITOL AND 2-AMINO-1,5-ANHYDRO-2-DEOXY-D-GLUCITOL
Witczak, Zbigniew J.,Whistler, Roy L.
, p. 121 - 132 (2007/10/02)
6-Amino-1,5-anhydro-6-deoxy-D-glucitol (11) was prepared from 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide (1) in six steps.Reduction of 1 with tributyltin hydride, followed by deacetylation, monomolar tosylation, and reacetylation, afforded 2,3,4-tr
