74016-19-6 Usage
Uses
Used in the Chemical Industry:
2-[(1E)-dec-1-en-1-yl]cyclopentanone serves as a key building block in organic synthesis, contributing to the preparation of a wide range of other organic compounds. Its unique structure allows for the creation of diverse chemical entities, enhancing the scope of chemical research and development.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, 2-[(1E)-dec-1-en-1-yl]cyclopentanone is utilized in the production of various drugs. Its distinctive chemical properties make it a valuable component in the synthesis of medicinal compounds, potentially leading to the development of new therapeutic agents.
Used in the Food Industry:
2-[(1E)-dec-1-en-1-yl]cyclopentanone is employed as a flavoring agent in the food industry, capitalizing on its strong and distinct odor. It adds unique flavor profiles to food products, enhancing the sensory experience for consumers.
Used in the Fragrance and Perfume Industry:
2-[(1E)-dec-1-en-1-yl]cyclopentanone also finds application in the formulation of fragrances and perfumes. Its distinct scent profile contributes to the creation of various olfactory compositions, enriching the world of fragrances and personal care products.
Check Digit Verification of cas no
The CAS Registry Mumber 74016-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,1 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74016-19:
(7*7)+(6*4)+(5*0)+(4*1)+(3*6)+(2*1)+(1*9)=106
106 % 10 = 6
So 74016-19-6 is a valid CAS Registry Number.
74016-19-6Relevant academic research and scientific papers
Desulfurization / α-Alkylation of β-Keto Sulfones
Kurth, Mark, J.,O'Brien, Michael, J.
, p. 3846 - 3848 (2007/10/02)
A one-pot procedure for the reductive alkylation of β-keto sulfones is described.The method proceeds by a lithium in liquid ammonia desulfurization of the starting β-keto sulfone, resulting in regiospecific generation of an intermediate enolate.Subsequent
