4041-11-6 Usage
Uses
Used in Flavor and Fragrance Industry:
2,5-dimethylcyclopent-2-en-1-one is utilized as a key ingredient in the creation of flavors and fragrances, capitalizing on its naturally sweet and fruity scent. Its ability to enhance the aroma profiles of various products makes it a valuable addition to the food and perfume industries.
Used in Organic Synthesis:
2,5-dimethylcyclopent-2-en-1-one serves as a building block in the synthesis of a wide range of organic compounds and pharmaceuticals. Its reactive ketone group and the presence of methyl groups on the cyclopentene ring make it a versatile intermediate for chemical reactions, facilitating the production of diverse molecules with potential applications in medicine and other fields.
Used in Pharmaceutical Research:
2,5-dimethylcyclopent-2-en-1-one has demonstrated potential as an antimicrobial and anti-inflammatory agent in some studies. Its ability to combat microbial infections and reduce inflammation positions it as a subject of interest for further research and development in the pharmaceutical sector, with the aim of discovering new treatments and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 4041-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4041-11:
(6*4)+(5*0)+(4*4)+(3*1)+(2*1)+(1*1)=46
46 % 10 = 6
So 4041-11-6 is a valid CAS Registry Number.
4041-11-6Relevant academic research and scientific papers
Palladium-Catalyzed Three Carbon Chain Extension Reactions with Acrolein Acetals. A Convenient Synthesis of Conjugated Dienals
Patel, Babu A.,Kim, Jin-Il I.,Bender, Diana D.,Kao, Lien-Chung,Heck, Richard F.
, p. 1061 - 1067 (2007/10/02)
A variety of vinylic halides has been found to react with acrolein or methacrolein acetals and amines with palladium catalysts to form 5-amino 3-enal acetals and/or dienal acetals.The reaction products yield 2,4-dienals on treatment with aqueous acids, in moderate to good yields.Crotonaldehyde dimethyl acetal also undergoes the reaction, but only in low yields. 3-Buten-2-one ethylene ketal reacted well under the same conditions, however, and Hofmann elimination and hydrolysis of the product amine gave (E,E)-3,5-heptadien-2-one in 90percent yield.
