28056-54-4 Usage
Uses
Used in Solvent Applications:
2,2,4-Trimethylcyclopentanone is utilized as a solvent in numerous industrial processes due to its ability to dissolve a broad range of substances, enhancing the efficiency and effectiveness of these operations.
Used in Fragrance Industry:
As a fragrance ingredient, 2,2,4-Trimethylcyclopentanone is employed for its unique odor profile, contributing to the creation of diverse and appealing scents in perfumes, cosmetics, and other fragrance-based products.
Used in Flavor and Fragrance Production:
2,2,4-Trimethylcyclopentanone is used as a key component in the production of flavors and fragrances, capitalizing on its distinctive scent to develop a variety of aromas for food, beverages, and other consumer goods.
Used in Pharmaceutical Applications:
2,2,4-Trimethylcyclopentanone has been investigated for its potential use in pharmaceutical products, suggesting that it may play a role in the development of new medications or drug delivery systems.
Used in Agricultural Applications:
2,2,4-TRIMETHYLCYCLOPENTANONE is also being explored for its possible applications in agriculture, indicating that it could be utilized in the development of pesticides, herbicides, or other agrochemicals to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 28056-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,5 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28056-54:
(7*2)+(6*8)+(5*0)+(4*5)+(3*6)+(2*5)+(1*4)=114
114 % 10 = 4
So 28056-54-4 is a valid CAS Registry Number.
28056-54-4Relevant academic research and scientific papers
Alternative synthesis of 2-hydroxy-3,5,5-trimethylcyclopent-2-en-1-one
Chapuis, Christian,Saint-Leger, Christine
scheme or table, p. 111 - 117 (2010/04/01)
The 2-hydroxy-3,5,5-trimethylcyclopent-2-en-1-one (1) was synthesized in 42% yield by rearrangement of epoxy ketone 10 on treatment with BF3 ? Et2O under anhydrous conditions. Intermediate 10 was available from the known enone 8, either via direct epoxidation (60% H2O 2 , NaOH, MeOH; yield 50%), or via reduction to the corresponding allylic alcohol 14 (LiAlH4, THF), followed by epoxidation ([VO(acac)2], tBuOOH) and reoxidation under Swern conditions, in 37% total yield.
Trisubstituted Stannyllithium as a Double Electron Equivalent. Reaction with α,β-Enones
Sato, Tadashi,Watanabe, Masami,Watanabe, Toshiyuki,Onoda, Yasuo,Murayama, Eigoro
, p. 1894 - 1899 (2007/10/02)
β-Stannyl ketones, easily available by the conjugate addition of (trimethylstannyl)lithium to α,β-enones, produced two types of ketones depending upon the substitution pattern by the treatment with titanium(IV) chloride.All the reactions proceeded through an intermediacy of cyclopropanol derivatives.The reaction involving the carbon skeleton rearrangement is promising as a synthetic method.
