6708-37-8 Usage
Uses
Used in Pharmaceutical Industry:
Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is used as a key intermediate in the synthesis of various pharmaceuticals due to its reactive nature and structural features, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides, enhancing their effectiveness in crop protection and agricultural management.
Used in Polymer Industry:
Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is employed as a crosslinking agent in the production of epoxy resins, improving the mechanical properties and thermal stability of the resulting polymers.
Used as a Curing Agent:
The anhydride form of the compound is used as a curing agent for various polymers, facilitating the formation of three-dimensional networks and enhancing the overall performance of the polymeric materials.
Used as a Hardener for Epoxy Resins:
Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is used as a hardener for epoxy resins, providing improved hardness, strength, and durability to the final product.
Used as an Antioxidant in Plastics:
In the plastics industry, the compound serves as an antioxidant, preventing the degradation of plastic materials and extending their service life.
Used as a Reactive Diluent in Adhesives and Coatings:
Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is used as a reactive diluent in adhesives and coatings, reducing the viscosity of the formulations and improving their application properties.
Used in the Synthesis of Fine Chemicals:
Due to its versatile reactivity and structural features, bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is employed as an intermediate in the synthesis of a wide range of fine chemicals, contributing to the development of specialty products with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6708-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6708-37:
(6*6)+(5*7)+(4*0)+(3*8)+(2*3)+(1*7)=108
108 % 10 = 8
So 6708-37-8 is a valid CAS Registry Number.
6708-37-8Relevant academic research and scientific papers
PHARMACEUTICAL COMPOSITION FOR USE IN THE TREATMENT AND PREVENTION OF ORTHOPOXVIRUS INFECTIONS AND ASSOCIATED DISEASES
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Paragraph 0095; 0096, (2016/08/03)
Pharmaceutical compositions containing di, tri, and tetracyclic acylhydrazide derivatives of the formula below, for use in the treatment or prophylaxis of viral infections and diseases associated therewith, particularly those viral infections and associated diseases caused by the orthopoxvirus.
Catalyst economy. Part 2: Sequential metathesis - Kharasch sequences using the Grubbs metathesis catalysts
Edlin, Chris D.,Faulkner, James,Quayle, Peter
, p. 1145 - 1151 (2007/10/03)
Sequential ring-closing metathesis (RCM)-Kharasch cyclizations are promoted by the Grubbs metathesis catalysts and provide rapid access to bicyclic lactones and lactams.
A Remarkably Efficient Photochemical Methodology for Endo to Exo Isomerization of Diels-Alder Cycloadducts
Pandey, Bipin,Athawale, Asawari A.,Reddy, Ravinder S.,Dalvi, Pramod V.,Kumar, Pradeep
, p. 1173 - 1176 (2007/10/02)
Irradiation of a solution of ethanol containing Diels-Alder cycloadducts and 10-20 percent (by volume) triethylamine at 300 nm furnishes quantitative yield (>90percent) of corresponding exo isomers.A probable mechanism based on photo-induced electron transfer (PET) has been described.
Synthesis of exo-Bicyclooct-5-ene-dicarboxylic Anhydrides by Thermal Isomerization of trans-Diacids
Weisz, Adrian,Mandelbaum, Asher
, p. 5812 - 5815 (2007/10/02)
Bicyclooct-5-ene-trans-1,2-dicarboxylic acid and substituted analogues afford mixtures of the corresponding exo- and endo-anhydrides upon heating at 250-300 deg C.This isomerization provides a practical pathway to substituted and deuterium-labeled exo-anhydrides which are otherwise difficult to obtain.A mechanistic study shows that retro-diene fragmentation is not involved in the isomerization.
