818-67-7 Usage
Description
METHALLYL ACRYLATE is a chemical compound with the molecular formula C8H12O2. It is a colorless liquid with a pungent odor, known for its rapid polymerization ability, making it a valuable ingredient in the production of various polymers, adhesives, coatings, and specialty chemicals.
Uses
Used in Polymer Production Industry:
METHALLYL ACRYLATE is used as a monomer for the production of polymers such as resins and plastics. Its rapid polymerization ability contributes to the efficient manufacturing process of these materials.
Used in Adhesive and Coating Industry:
METHALLYL ACRYLATE is used as a key ingredient in the formulation of adhesives and coatings due to its fast polymerization properties, which enhance the bonding and protective qualities of these products.
Used in Specialty Chemicals Synthesis:
METHALLYL ACRYLATE is used as a component in the synthesis of specialty chemicals, where its unique properties can be leveraged to create novel compounds with specific applications.
Used in Consumer Product Manufacturing:
METHALLYL ACRYLATE is used as a component in the manufacturing of various consumer products, where its polymerization properties can contribute to the development of innovative and improved materials.
It is important to handle METHALLYL ACRYLATE with caution, as it can be irritating to the skin, eyes, and respiratory system, and exposure to high concentrations of the compound can have harmful effects on human health.
Check Digit Verification of cas no
The CAS Registry Mumber 818-67-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 818-67:
(5*8)+(4*1)+(3*8)+(2*6)+(1*7)=87
87 % 10 = 7
So 818-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O2/c1-4-7(8)9-5-6(2)3/h4H,1-2,5H2,3H3
818-67-7Relevant articles and documents
Chiral hetero- and carbocyclic compounds from the asymmetric hydrogenation of cyclic alkenes
Verendel, J. Johan,Li, Jia-Qi,Quan, Xu,Peters, Byron,Zhou, Taigang,Gautun, Odd R.,Govender, Thavendran,Andersson, Pher G.
supporting information; experimental part, p. 6507 - 6513 (2012/06/29)
Several types of chiral hetero- and carbocyclic compounds have been synthesized by using the asymmetric hydrogenation of cyclic alkenes. N,P-Ligated iridium catalysts reduced six-membered cyclic alkenes with various substituents and heterofunctionality in good to excellent enantioselectivity, whereas the reduction of five-membered cyclic alkenes was generally less selective, giving modest enantiomeric excesses. The stereoselectivity of the hydrogenation depended more strongly on the substrate structure for the five- rather than the six-membered cyclic alkenes. The major enantiomer formed in the reduction of six-membered alkenes could be predicted from a selectivity model and isomeric alkenes had complementary enantioselectivity, giving opposite optical isomers upon hydrogenation. The utility of the reaction was demonstrated by using it as a key step in the preparation of chiral 1,3-cis-cyclohexane carboxylates. Copyright
Selective enzymatic epoxidation of dienes: Generation of functional enantiomerically enriched diene monoepoxy monomers
Hu, Shanghui,Gupta, Pankaj,Prasad, Ashok K,Gross, Richard A,Parmar, Virinder S
, p. 6763 - 6766 (2007/10/03)
Enantiomerically enriched diene monoepoxides were selectively synthesized using oxidases from Pseudomonas sp. and chloroperoxidase from Caldariomyces fumago. These monoepoxides are useful monomers for generating functional chiral polymeric materials.
