10471-78-0 Usage
Description
2-Isopropenyl-2-oxazoline 99+% is an organic compound that is primarily utilized in the polymer industry for the functionalization of polypropylene. 2-ISOPROPENYL-2-OXAZOLINE 99+% is known for its high purity, with a percentage of 99+%, which ensures its effectiveness and reliability in various applications.
Uses
Used in Polymer Industry:
2-Isopropenyl-2-oxazoline 99+% is used as a functionalizing agent for polypropylene to enhance its compatibility with other materials. The application reason is to improve the properties of polypropylene and make it more suitable for use in various industries.
Used in Rubber Industry:
2-Isopropenyl-2-oxazoline 99+% is used as a compatibilizer for PP/(acrylonitrile-co-butadiene-co-acrylic acid) rubber (NBR) blends. The application reason is to improve the compatibility and performance of the blend, resulting in enhanced mechanical properties and overall performance of the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 10471-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10471-78:
(7*1)+(6*0)+(5*4)+(4*7)+(3*1)+(2*7)+(1*8)=80
80 % 10 = 0
So 10471-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO/c1-5(2)6-7-3-4-8-6/h1,3-4H2,2H3
10471-78-0Relevant articles and documents
Asymmetric hetero-Diels-Alder reactions of alkenyldihydrooxazoles. Synthesis of oxazolo[3,2-c]pyrimidines and related compounds
Elliott, Mark C.,Kruisvvijk, Elbertus
, p. 3157 - 3166 (1999)
Alkenyldihydrooxazoles undergo a highly diastereoselective formal aza-Diels-Alder reaction with aryl and arenesulfonyl isocyanates to give oxazolo[3,2-c]pyrimidines. Depending on the substitution pattern of the alkenyldihydrooxazole, these compounds may then undergo addition of a second equivalent of the isocyanate to give either tetrahydrooxazoIo[3,2-c]pyrimidine-8-carboxamides or octahydroazeto[2,3-7]oxazolo[3,2c]pyrimidines. The second addition is sensitive to steric and electronic factors, and can be prevented in some cases. The Royal Society of Chemistry 1999.
