7089-59-0 Usage
Uses
Used in Adhesives Industry:
2,4-O-(furan-2-ylmethylidene)hexitol is used as a reactive diluent for [application reason] its high reactivity and ability to form strong bonds, enhancing the performance and durability of adhesives.
Used in Coatings Industry:
In the coatings industry, 2,4-O-(furan-2-ylmethylidene)hexitol is used as a key component in the formulation of high-performance coatings, contributing to improved adhesion, durability, and resistance to environmental factors.
Used in Pharmaceuticals Industry:
2,4-O-(furan-2-ylmethylidene)hexitol is utilized as an intermediate in the synthesis of pharmaceutical compounds, leveraging its reactivity and bonding capabilities to create novel drug molecules with potential therapeutic applications.
Used in Polymer and Resin Synthesis:
As a building block in polymer and resin synthesis, 2,4-O-(furan-2-ylmethylidene)hexitol is used for [application reason] its ability to form strong, stable polymer structures, which are essential in creating materials with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7089-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7089-59:
(6*7)+(5*0)+(4*8)+(3*9)+(2*5)+(1*9)=120
120 % 10 = 0
So 7089-59-0 is a valid CAS Registry Number.
7089-59-0Relevant academic research and scientific papers
2,4-Furfurylidene-D-sorbitol and its tetra-methyl ether: Synthesis, conformational studies, and radical scavenging activity
Ciuffreda, Pierangela,Brizzolari, Andrea,Casati, Silvana,Eberini, Ivano,Palazzolo, Luca,Parravicini, Chiara,Santaniello, Enzo
, p. 50 - 68 (2016/10/31)
The structure of 1-[2-(furan-2-yl)-5-hydroxy-6-(hydroxymethyl)-1,3-dioxan-4-yl]ethane-1,2-diol] (2,4-furfurylidene-D-sorbitol) and its tetra-methyl ether was established by a detailed NMR analysis. The conformational structure for both compounds was confirmed by in silico studies based both on Density Functional Theory (DFT) and on classical molecular dynamics approaches. The scavenging activity against hydroxyl radicals (?OH) of compounds was established by the 2 deoxyribose degradation assay.
