19969-71-2 Usage
Description
2,5-Dihydro-2,5-dimethoxyfurfuryl alcohol, a chemical compound with the molecular formula C8H12O4, is a colorless liquid characterized by a sweet, fruity odor. It is recognized for its potential biological activities, such as antioxidant and anti-inflammatory properties, which are currently under investigation.
Uses
Used in Food and Beverage Industry:
2,5-Dihydro-2,5-dimethoxyfurfuryl alcohol is used as a flavoring agent for its distinctive sweet, fruity scent, enhancing the taste profiles of various food and beverage products.
Used in Cosmetic and Personal Care Industry:
In the cosmetic and personal care sector, 2,5-Dihydro-2,5-dimethoxyfurfuryl alcohol serves as a fragrance ingredient, adding pleasant aromas to products and improving the sensory experience for consumers.
Used in Pharmaceutical and Nutraceutical Industry:
Given its potential antioxidant and anti-inflammatory properties, 2,5-Dihydro-2,5-dimethoxyfurfuryl alcohol is being studied for possible applications in the development of pharmaceutical and nutraceutical products aimed at promoting health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 19969-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19969-71:
(7*1)+(6*9)+(5*9)+(4*6)+(3*9)+(2*7)+(1*1)=172
172 % 10 = 2
So 19969-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O4/c1-9-6-3-4-7(5-8,10-2)11-6/h3-4,6,8H,5H2,1-2H3
19969-71-2Relevant articles and documents
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Tanaka et al.
, p. 3482 (1976)
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Electroorganic synthesis of 2,5-dialkoxydihydrofurans and pyridazines on solid phase using polymer beads as supports
Nad, Sukanya,Breinbauer, Rolf
, p. 3654 - 3665 (2005)
Electroorganic synthesis has defied application in Solid-Phase Organic Synthesis (SPOS) so far. Typically more than 99.9% of the substrate molecules immobilized on a polymeric support are buried in the interior of the bead, and therefore are unable to undergo direct contact with a heterogeneous reagent such as an electrode. This intrinsic impediment for an electrochemical reaction can be overcome by the use of a redox mediator which shuttles electrons from the electrode to the polymer bound substrate molecules. This approach of indirect electroorganic synthesis was successfully applied for the 2,5-dialkoxylation of furans on solid phase. The oxidation products can be hydrolyzed and through condensation with hydrazine hydrate substituted pyridazines are produced in 50-65% overall yield. Georg Thieme Verlag Stuttgart.
The first de novo-designed antagonists of the human NK2 receptor
Ali, Mohammed A.,Bhogal, Nirmala,Findlay, John B. C.,Fishwick, Colin W. G.
, p. 5655 - 5658 (2005)
The de novo molecular design program SPROUT has been used in conjunction with a molecular model to produce a molecular template for a new class of NK2 receptor antagonist. An efficient, stereocontrolled synthesis of a small series of molecules,
