13241-36-6 Usage
Description
1,4:3,6-Dianhydro-D-threo-hexo-2,5-diulose, commonly known as isosorbide, is a heterocyclic compound derived from glucose. It is a versatile building block for polymers, particularly in the production of biodegradable plastics, and serves as a sustainable and environmentally friendly alternative to traditional petrochemical-based plastics. In the pharmaceutical industry, isosorbide is utilized in the development of certain medications, including vasodilators and diuretics, and is under investigation for its potential therapeutic effects in treating various medical conditions such as cardiovascular disease and cancer.
Uses
Used in Plastics Industry:
1,4:3,6-Dianhydro-D-threo-hexo-2,5-diulose is used as a monomer for the production of biodegradable plastics, offering a more sustainable and environmentally friendly option compared to traditional petrochemical-based plastics.
Used in Pharmaceutical Industry:
1,4:3,6-Dianhydro-D-threo-hexo-2,5-diulose is used as an active pharmaceutical ingredient in the production of certain medications, such as vasodilators and diuretics, due to its potential therapeutic effects.
Used in Research and Development:
1,4:3,6-Dianhydro-D-threo-hexo-2,5-diulose is used as a subject of research for its potential therapeutic effects in the treatment of various medical conditions, including cardiovascular disease and cancer, as it is being investigated for its possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 13241-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13241-36:
(7*1)+(6*3)+(5*2)+(4*4)+(3*1)+(2*3)+(1*6)=66
66 % 10 = 6
So 13241-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O4/c7-3-1-9-6-4(8)2-10-5(3)6/h1-2,5-8H
13241-36-6Relevant articles and documents
Method for Direct Synthesis of Isosorbide Diketone from Isosorbide Using (2,2,6,6-Tetramethylpiperidin-1-yl)oxyl-based Derivatives and Transition Metal Nitrates
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Paragraph 0094-0099; 0115-0121, (2020/04/17)
According to an embodiment of the present disclosure, provided are: a (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO)-based derivative; and a method for direct synthesizing isosorbide diketone from isosorbide under mild reaction conditions without using highly toxic and corrosive acid components by improving reaction mechanism by a catalyst system comprising nitrates of a transition metal.COPYRIGHT KIPO 2020
Aerobic oxidation of isosorbide and isomannide employing TEMPO/laccase
Gross, Johannes,Tauber, Katharina,Fuchs, Michael,Schmidt, Nina G.,Rajagopalan, Aashrita,Faber, Kurt,Fabian, Walter M. F.,Pfeffer, Jan,Haas, Thomas,Kroutil, Wolfgang
, p. 2117 - 2121 (2014/04/17)
The oxidation of the renewable diols isosorbide and isomannide was successfully achieved using a TEMPO/laccase system. Furthermore, various TEMPO-derivatives were tested leading to conversions of up to >99% for the oxidation of isosorbide, isomannide, indanol and a halohydrin to the corresponding ketone. the Partner Organisations 2014.
METHOD FOR PRODUCING ALDEHYDES AND KETONES FROM PRIMARY AND SECONDARY ALCOHOLS
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Page/Page column 5, (2011/10/19)
The invention relates to a method for producing aldehydes and ketones from easily accessible primary and secondary alcohols by oxidation with atmospheric oxygen or pure oxygen using a catalyst system which consists of a derivative of a free nitroxyl radical.
