2807-54-7 Usage
Uses
Used in Polymer and Resin Production:
Diallyl fumarate is used as a crosslinking agent for enhancing the strength and stability of polymers and resins. Its high reactivity allows for the formation of strong bonds between polymer chains, contributing to the improved performance of the final product.
Used in High-Temperature-Resistant Materials:
Diallyl fumarate is utilized as a key component in the manufacturing of materials that can withstand high temperatures. Its excellent heat resistance makes it suitable for applications requiring durability and stability under extreme thermal conditions.
Used in Adhesives and Coatings:
Diallyl fumarate is employed as a critical ingredient in the production of adhesives and coatings. Its ability to form strong bonds and offer heat resistance makes it an ideal choice for creating long-lasting and temperature-resistant adhesives and coatings.
Used in Dental Composites:
In the dental industry, diallyl fumarate is used in the formulation of dental composites. Its properties contribute to the development of dental materials with enhanced durability and resistance to wear.
Used in Electrical Insulation Materials:
Diallyl fumarate is incorporated into the production of electrical insulation materials. Its heat resistance and mechanical properties ensure the safety and reliability of electrical systems by preventing electrical leakage and short circuits.
Used in Structural Adhesives:
Diallyl fumarate is used as a component in structural adhesives. Its strong bonding capabilities and heat resistance make it suitable for applications requiring durable and temperature-resistant adhesives in construction and manufacturing.
Used in the Food Industry:
Diallyl fumarate is used as a flavoring and fragrance agent in the food industry. Its ability to impart specific tastes and scents adds value to various food products, enhancing their appeal to consumers.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, diallyl fumarate is utilized for drug delivery systems. Its properties allow for the controlled release of drugs, improving the efficacy and safety of pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 2807-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2807-54:
(6*2)+(5*8)+(4*0)+(3*7)+(2*5)+(1*4)=87
87 % 10 = 7
So 2807-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4/c1-3-7-13-9(11)5-6-10(12)14-8-4-2/h3-6H,1-2,7-8H2/b6-5+
2807-54-7Relevant academic research and scientific papers
Zwitterion-Catalyzed Isomerization of Maleic to Fumaric Acid Diesters
Lam, Ying-Pong,Lam, Zachary,Yeung, Ying-Yeung
, p. 1183 - 1190 (2021/01/09)
Fumaric acid diesters are important building blocks for organic synthesis. A class of zwitterionic organocatalysts based on an amide anion/iminium cation charge pair were found to be effective in catalyzing the isomerization of maleic acid diesters to give fumaric acid diesters. Comparison of the performance of different zwitterionic organocatalysts toward the reaction revealed that nonclassical hydrogen bonding was involved in the stabilization of the Michael adduct intermediate.
Conjugate addition/Ireland-Claisen rearrangements of allyl fumarates: Simple access to terminally differentiated succinates
Bausch, Cory C.,Johnson, Jeffrey S.
, p. 1575 - 1577 (2008/09/17)
(Chemical Equation Presented) The conjugate addition of dialkylzinc reagents to allyl fumarates with subsequent Ireland-Claisen rearrangement has been accomplished yielding substituted unsymmetrical succinic acid derivatives. This one-pot reaction creates two new carbon-carbon bonds at contiguous stereogenic centers. The reaction proceeds for several alkylzinc reagents and substituted allyl fumarates. The products contain distinguishable functional handles for further manipulation.
Macrocyclic Thia-alkenolides Formed by Intramolecular 'Ene'Reactions of Thioaldehydes
Choi, Samuel S.-M.,Kirby, Gordon W.,Mahajan, Mohinder P.
, p. 191 - 198 (2007/10/02)
The crystalline acids which are formally cycloadducts of cyclopentadiene and the thioaldehyde thioxoacetic acid (HO2C-CHS) have been converted into a series of esters with the alkenols CH2=CHnOH.These cycloadduct esters, 8 and 9, when subjected to flash vacuum pyrolysis (FVP) at ca. 500 deg C, liberated the corresponding alkenyl thioacetates, 10, which underwent intramolecular 'ene'reactions to give a series of thia-alkenolides having 6- to 11-membered rings.The 3-thianon-5-en-9-olide 11d has been transformed, by standard reactions, into 3-vinylhex-2-en-6-olide, 20, with removal of sulfur.The sulfoxides 28 of the cyclopentadiene adducts have been employed similarly as precursors for the corresponding thioxoacetate ester S-oxides (sulfines).Under FVP conditions, intramolecular cyclisation of the allyl 33 and the homoallyl 29 sulfines gave furan-2(5H)-one 35 and 5,6-dihydro-2-pyrone, 31, respectively.The prenyl derivative 37 gave a mixture of the simple product furan-2(5H)-one 35 and its 4-isopropenyl derivative 39.Generally, fumarate esters were formed from sulfines that had failed to cyclise.
