2247206-06-8 Usage
Description
(4S,4's)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-phenyl-4,5-dihydro-oxazole) is a complex chemical compound that features a bisphenol A backbone and two oxazole rings. As a bisphenol derivative, it is related to compounds used in the production of polycarbonate plastics and epoxy resins. The unique structure of this compound suggests potential applications in material manufacturing, although it is distinct from traditional bisphenol A due to its specific modifications.
Uses
Used in Plastics Industry:
(4S,4's)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-phenyl-4,5-dihydro-oxazole) is used as a specialty chemical in the plastics industry for its potential role in enhancing or modifying the properties of polycarbonate plastics. Its unique structure may offer specific advantages over traditional bisphenol A, such as improved thermal stability, mechanical strength, or resistance to environmental factors.
Used in Epoxy Resin Production:
In the epoxy resin industry, (4S,4's)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-phenyl-4,5-dihydro-oxazole) is utilized as a curative or hardener to improve the cross-linking process and the final properties of the epoxy resins. Its incorporation may lead to epoxy resins with superior adhesion, electrical insulation, or chemical resistance, which are crucial for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2247206-06-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,2,4,7,2,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2247206-06:
(9*2)+(8*2)+(7*4)+(6*7)+(5*2)+(4*0)+(3*6)+(2*0)+(1*6)=138
138 % 10 = 8
So 2247206-06-8 is a valid CAS Registry Number.
2247206-06-8Relevant articles and documents
A chiral cagelike copper(I) catalyst for the highly enantioselective synthesis of 1,1-cyclopropane diesters
Deng, Chao,Wang, Li-Jia,Zhu, Jun,Tang, Yong
supporting information, p. 11620 - 11623,4 (2012/12/12)
Triangulation method: The catalytic enantioselective cyclopropanation of multisubstituted olefins with phenyliodonium ylide malonate has been achieved in the presence of a chiral bisoxazoline copper(I) complex (see scheme). A wide range of substrates undergo the reaction to provide optically active 1,1-cyclopropane diesters in high yield with up to >99 %-ee. A rationale for the enantioselective induction has been proposed. Copyright
