23643-29-0 Usage
Description
1,6-Anhydro-4-O-toluenesulfonyl-β-D-glucopyranose, often abbreviated as 1,6-ANHYDRO, is a specialized chemical compound derived from β-D-glucopyranose, a type of sugar. It is characterized by its white solid appearance and is known for its unique chemical properties, which make it valuable in various industrial applications.
Uses
Used in Pharmaceutical Industry:
1,6-ANHYDRO is used as an intermediate in the synthesis of complex carbohydrate structures for pharmaceutical applications. Its unique chemical properties allow for the creation of novel drug candidates with potential therapeutic benefits.
Used in Chemical Synthesis:
1,6-ANHYDRO is used as a key building block in the synthesis of various anhydro sugars, which are important components in the development of new chemical compounds and materials. Its versatility in chemical reactions makes it a valuable asset in the field of organic chemistry.
Used in Research and Development:
1,6-ANHYDRO is utilized as a research tool in the study of carbohydrate chemistry and its role in biological systems. Its unique structure provides insights into the mechanisms of carbohydrate interactions and can lead to the discovery of new biological processes and potential therapeutic targets.
Used in Material Science:
1,6-ANHYDRO is employed in the development of advanced materials, such as polymers and coatings, that leverage the unique properties of anhydro sugars. Its incorporation into these materials can result in improved performance characteristics, such as enhanced stability and resistance to degradation.
Check Digit Verification of cas no
The CAS Registry Mumber 23643-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,4 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23643-29:
(7*2)+(6*3)+(5*6)+(4*4)+(3*3)+(2*2)+(1*9)=100
100 % 10 = 0
So 23643-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O7S/c1-7-2-4-8(5-3-7)21(16,17)20-12-9-6-18-13(19-9)11(15)10(12)14/h2-5,9-15H,6H2,1H3/t9-,10-,11-,12-,13-/m1/s1
23643-29-0Relevant articles and documents
Efficient synthesis of a galectin inhibitor clinical candidate (TD139) using a Payne rearrangement/azidation reaction cascade
Denavit, Vincent,Giguère, Denis,St-Gelais, Jacob
supporting information, p. 3903 - 3907 (2020/06/03)
Selective galectin inhibitors are valuable research tools and could also be used as drug candidates. In that context, TD139, a thiodigalactoside galectin-3 inhibitor, is currently being evaluated clinically for the treatment of idiopathic pulmonary fibrosis. Herein, we describe a new strategy for the preparation of TD139. Starting from inexpensive levoglucosan, we used a rarely employed reaction cascade: Payne rearrangement/azidation process leading to 3-azido-galactopyranose. The latter intermediate was efficiently converted into TD139 in a few simple and practical steps.
Exploring the Chemistry of Non-sticky Sugars: Synthesis of Polyfluorinated Carbohydrate Analogues of d-Allopyranose
Denavit, Vincent,St-Gelais, Jacob,Tremblay, Thomas,Giguère, Denis
supporting information, p. 9272 - 9279 (2019/07/05)
There is a growing interest in the preparation of polyfluorinated carbohydrates. A limited number of fluorohexopyranosides have been used in biological investigations because of the synthetic challenge they present. Hence, we report the synthesis of fluor
1H NMR STUDY OF 1,6-ANHYDRO-β-D-GLUCOPYRANOSE TOSYLATED AT 2- AND/OR 4-POSITION
Rijsbergen, Ronan Van,Anteunis, Marc J. O.,Bruyn, Andre De
, p. 297 - 300 (2007/10/02)
The 1H nmr spectra of 1,6-anhydro-2-O-tosyl-, 1,6-anhydro-4-O-tosyl and 1,6-anhydro-2,4-di-O-tosyl-β-D-glucopyranose have been analyzed.The data allow to discriminate between the two monosubstituted levoglucosans.
