22595-45-5 Usage
General Description
2,2,4,4-Tetramethyl-6-(2-methyl-1-oxopropyl)-1,3,5-cyclohexanetrione, also known as Trolox, is a synthetic derivative of vitamin E and an antioxidant compound. It has a chemical structure similar to that of vitamin E, and is used in various industries such as food, cosmetics, and pharmaceuticals. Trolox has been found to have powerful antioxidant properties, and it is often used to stabilize and protect sensitive molecules from oxidative damage. It has also been studied for its potential to prevent or delay the onset of certain age-related diseases and conditions. Additionally, Trolox has shown promise in research for its potential anti-inflammatory and anti-cancer properties. Overall, 2,2,4,4-Tetramethyl-6-(2-methyl-1-oxopropyl)-1,3,5-cyclohexanetrione is a versatile and valuable chemical compound with a wide range of potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 22595-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22595-45:
(7*2)+(6*2)+(5*5)+(4*9)+(3*5)+(2*4)+(1*5)=115
115 % 10 = 5
So 22595-45-5 is a valid CAS Registry Number.
22595-45-5Relevant articles and documents
Total synthesis of a monomeric phloroglucinol derivative isolated from Myrtus communis
Nishimura, Eiji,Ohfune, Yasufumi,Shinada, Tetsuro
, p. 445 - 447 (2015)
The first total synthesis of a monomeric phloroglucinol [(1R,2S)-2-hydroxy-2-isobutyl-4,4,6,6-tetramethyl-3,5-dioxocyclohexyl acetate] was achieved by stereoselective reduction of a symmetrical α-ketol as a key step. The corresponding cis-stereoisomer of
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and e
Cheng, Min-Jing,Cao, Jia-Qing,Yang, Xin-Yi,Zhong, Li-Ping,Hu, Li-Jun,Lu, Xi,Hou, Bao-Long,Hu, Ya-Jian,Wang, Ying,You, Xue-Fu,Wang, Lei,Ye, Wen-Cai,Li, Chuang-Chuang
, p. 1488 - 1495 (2018/02/14)
Herein, we describe a concise catalytic approach to the first asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E. The syntheses proceed in only 5-7 steps from the readily available compound 11, witho
