6731-86-8 Usage
Description
1,1-BIS(TERT-BUTYLPEROXY)-3,3,5-TRIMETHYLCYCLOHEXANE is a highly reactive organic peroxide compound commonly used as a polymerization initiator in the production of various plastics, such as polystyrene and polyethylene. It rapidly decomposes to generate free radicals, which facilitate the polymerization process. Additionally, it is utilized as a crosslinking agent in the production of rubber and elastomers. Due to its instability and potential for explosive decomposition, it must be handled and stored with extreme caution under tightly controlled conditions to ensure safety and prevent accidents.
Uses
Used in Plastics Industry:
1,1-BIS(TERT-BUTYLPEROXY)-3,3,5-TRIMETHYLCYCLOHEXANE is used as a polymerization initiator for the production of various plastics, such as polystyrene and polyethylene. Its rapid decomposition to generate free radicals facilitates the polymerization process, enabling the creation of a wide range of plastic products.
Used in Rubber and Elastomers Industry:
1,1-BIS(TERT-BUTYLPEROXY)-3,3,5-TRIMETHYLCYCLOHEXANE is used as a crosslinking agent in the production of rubber and elastomers. Its ability to generate free radicals upon decomposition helps in forming the necessary crosslinks between polymer chains, enhancing the mechanical properties and performance of rubber and elastomer products.
Check Digit Verification of cas no
The CAS Registry Mumber 6731-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,3 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6731-86:
(6*6)+(5*7)+(4*3)+(3*1)+(2*8)+(1*6)=108
108 % 10 = 8
So 6731-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H24N2O3S/c1-3-22(20,21)18-11-9-15(10-12-18)16(19)17-13(2)14-7-5-4-6-8-14/h4-8,13,15H,3,9-12H2,1-2H3,(H,17,19)
6731-86-8Relevant articles and documents
Highly Enantioselective Synthesis of Indolines: Asymmetric Hydrogenation at Ambient Temperature and Pressure with Cationic Ruthenium Diamine Catalysts
Yang, Zhusheng,Chen, Fei,He, Yanmei,Yang, Nianfa,Fan, Qing-Hua
supporting information, p. 13863 - 13866 (2016/10/26)
A highly enantioselective synthesis of indolines by asymmetric hydrogenation of 1H-indoles and 3H-indoles at ambient temperature and pressure, catalyzed by chiral phosphine-free cationic ruthenium complexes, has been developed. Excellent enantio- and diastereoselectivities (up to >99 % ee, >20:1 d.r.) were obtained for a wide range of indole derivatives, including unprotected 2-substituted and 2,3-disubstituted 1H-indoles, as well as 2-alkyl- and 2-aryl-substituted 3H-indoles.
