2424-98-8 Usage
Uses
Used in Chemical Manufacturing:
Vinyl isobutyrate is used as a plasticizer for increasing the flexibility and workability of materials in the chemical industry. Its application enhances the properties of certain plastics, making them more suitable for specific uses.
Used in Pharmaceutical Industry:
Vinyl isobutyrate is used as an intermediate in the synthesis of various pharmaceutical compounds. Its role in the production process is crucial for creating the desired end products with the required therapeutic properties.
Used in Processing Aids:
Vinyl isobutyrate is used as a processing aid in the manufacturing of certain products, improving the efficiency and quality of the final output. It helps in facilitating the production process and achieving better results.
Used in Copolymer Synthesis:
Vinyl isobutyrate is used as a reactant in the synthesis of copolymers, which are polymers composed of two or more different monomers. Its involvement in the polymerization process contributes to the creation of materials with unique properties and applications.
Health Precautions:
While vinyl isobutyrate has various applications, it is essential to handle and store it with care due to its potential health risks. It may cause skin and eye irritation and can be harmful to the respiratory system if inhaled. Proper safety measures should be taken to minimize any potential hazards associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2424-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2424-98:
(6*2)+(5*4)+(4*2)+(3*4)+(2*9)+(1*8)=78
78 % 10 = 8
So 2424-98-8 is a valid CAS Registry Number.
2424-98-8Relevant academic research and scientific papers
Competitive reactivity as a probe for reaction coordinates in gas-phase ion-molecule chemistry
Holman, Robert W.,Sumpter, Terry L.,Farrar, John,Weigel, Kurt,Bartmess, John E.
, p. 585 - 589 (2007/10/03)
Using the method of competitive reactivity of two functional groups in the same molecule, anionic elimination reactions show considerable kinetic selectivity for small differences in leaving group thermochemistry, in structures of the general type YCH2CH2CH2Z, where Y and Z are good anionic leaving groups.
A novel synthesis of vinyl esters from vinylversatate-10
Mondal,Van Der Meer,German,Heikens
, p. 4205 - 4207 (2007/10/05)
Vinylversatate-10 (VV10)1 1 VV 10 Vinyl Monomer, Development Product, Shell Chemical Company has successfully been used to synthesise a large number of lower vinyl esters by transvinylation in presence of mercuric acetate and sulfuric acid. The synthesis of vinylhalo esters proceeds with more difficulty. It has been observed that neither Hg(OAc)2 nor H2SO4 alone is capable of initiating the transvinylation. Furthermore, it has been found that a molar ratio 2:1 of VV10 to carboxylic acid is sufficient to drive the reaction to the right by continuous distillation of the vinyl ester formed, and as a result a high yield of vinyl ester is obtained. A mechanism for this reaction and for the formation of side products has been proposed.
