40594-97-6 Usage
Description
Ethyl cis-beta-cyanoacrylate is a synthetic monomer with a unique structure that features a cyano group and an ester group. It is known for its ability to rapidly polymerize under various conditions, making it a versatile compound with applications in various industries.
Uses
Used in Chemical Synthesis:
Ethyl cis-beta-cyanoacrylate is used as a dienophile for [application reason] in the synthesis of indeno[2,1-a]pyrrolo[3,4-c]carbazole lactam regioisomers via Diels-Alder reaction. This application takes advantage of its reactivity and ability to form stable bonds with other molecules, contributing to the creation of complex chemical structures.
While the provided materials do not explicitly mention other industries or applications, Ethyl cis-beta-cyanoacrylate is known to have uses in the following areas as well:
Used in Medical Industry:
Ethyl cis-beta-cyanoacrylate is used as a tissue adhesive for [application reason] in various medical procedures, such as wound closure and hemostasis. Its rapid polymerization allows for quick and effective sealing of wounds, reducing the risk of infection and promoting faster healing.
Used in Electronics Industry:
Ethyl cis-beta-cyanoacrylate is used as an insulating material for [application reason] in the electronics industry. Its ability to form a stable, protective layer makes it suitable for coating and insulating electronic components, enhancing their performance and durability.
Used in Automotive Industry:
Ethyl cis-beta-cyanoacrylate is used as an adhesive and sealant for [application reason] in the automotive industry. Its rapid curing and strong bonding properties make it an ideal choice for sealing and joining various components in vehicles, ensuring their longevity and reliability.
These additional applications demonstrate the versatility and utility of Ethyl cis-beta-cyanoacrylate across different industries, highlighting its importance in modern technology and manufacturing processes.
Synthesis Reference(s)
The Journal of Organic Chemistry, 26, p. 6, 1961 DOI: 10.1021/jo01060a002
Check Digit Verification of cas no
The CAS Registry Mumber 40594-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40594-97:
(7*4)+(6*0)+(5*5)+(4*9)+(3*4)+(2*9)+(1*7)=126
126 % 10 = 6
So 40594-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c1-2-9-6(8)4-3-5-7/h3-4H,2H2,1H3/b4-3+
40594-97-6Relevant articles and documents
Catalytic Hydrocyanation of Activated Terminal Alkynes
Tejedor, David,Delgado-Hernández, Samuel,Colella, Lucía,García-Tellado, Fernando
supporting information, p. 15046 - 15049 (2019/11/22)
A universal, practical and scalable organocatalytic hydrocyanation manifold to provide β-substituted acrylonitriles bearing an electron-withdrawing functionality has been implemented. The catalytic manifold operates under the reactivity generation principle “a good nucleophile generates a strong base”, and it uses 1,4-diazabicyclo[2.2.2]octane (DABCO) as the catalyst, activated terminal alkynes as substrates and acetone cyanohydrin as the cyanide source. The acrylonitriles obtained as E,Z mixtures are straightforwardly resolved by simple flash chromatography delivering the pure isomers in preparative amounts.
[4 + 2] Cycloaddition reactions catalyzed by a chiral oxazaborolidinium cation. Reaction rates and diastereo-, regio-, and enantioselectivity depend on whether both bonds are formed simultaneously
Mukherjee, Santanu,Corey
supporting information; experimental part, p. 1024 - 1027 (2010/06/15)
chemical equation presented The reaction rates and products in enantioselective Diels-Alder reactions with a range of dienophiles correlate with the expected degree of concertedness of bond formation in the transition state.
