13912-65-7 Usage
Uses
Used in Organic Synthesis:
4-(2,5-DIOXOTETRAHYDROFURAN-3-YL)-1,2,3,4-TETRAHYDRONAPHTHALENE-1,2-DICARBOXYLIC ANHYDRIDE is used as a reagent and building block for the preparation of various pharmaceuticals and fine chemicals. Its unique structure allows it to be a key component in the synthesis of complex organic molecules, contributing to the development of new compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2,5-DIOXOTETRAHYDROFURAN-3-YL)-1,2,3,4-TETRAHYDRONAPHTHALENE-1,2-DICARBOXYLIC ANHYDRIDE is used as a starting material for the synthesis of new drug candidates. Its structural features make it a valuable intermediate in the development of novel therapeutic agents, potentially leading to the discovery of new medicines with improved efficacy and safety profiles.
Used in Material Science:
4-(2,5-DIOXOTETRAHYDROFURAN-3-YL)-1,2,3,4-TETRAHYDRONAPHTHALENE-1,2-DICARBOXYLIC ANHYDRIDE is also used in the development of new materials and chemical processes. Its properties may contribute to the creation of advanced materials with unique characteristics, such as improved stability, reactivity, or selectivity, which can be applied in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13912-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,1 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13912-65:
(7*1)+(6*3)+(5*9)+(4*1)+(3*2)+(2*6)+(1*5)=97
97 % 10 = 7
So 13912-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C32H26O13/c33-23-11-19(29(39)43-23)17-9-21(27(35)36)25(15-7-3-1-5-13(15)17)31(41)45-32(42)26-16-8-4-2-6-14(16)18(10-22(26)28(37)38)20-12-24(34)44-30(20)40/h1-8,17-22,25-26H,9-12H2,(H,35,36)(H,37,38)
13912-65-7Relevant academic research and scientific papers
Process for reacting maleic anhydride with vinylbenzenes
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, (2008/06/13)
The reaction of maleic anhydride with vinylbenzene to form tetralin dianhydride is improved by conducting, per mole of vinyl group, 2-20 l/h of air (measured under normal conditions: 20° C./l bar) through the reaction mixture.
