19781-29-4 Usage
Uses
Used in Food and Beverage Industry:
3-Ethyl-4-octanone is used as a flavoring agent to enhance the taste of products such as candy, baked goods, and fruit-flavored beverages, providing a sweet and fruity aroma that improves the overall sensory experience of these items.
Used in Perfumery:
In the fragrance industry, 3-Ethyl-4-octanone is used as a fragrance ingredient in perfumes and colognes, capitalizing on its pleasant scent to contribute to the creation of desirable and long-lasting fragrances.
Used in Pharmaceutical Production:
3-Ethyl-4-octanone also finds application in the production of pharmaceuticals, where it may be utilized in the synthesis of various medicinal compounds or as a component in the formulation of drugs.
Used as an Industrial Solvent:
Furthermore, 3-Ethyl-4-octanone serves as a solvent in a range of industrial processes, where its properties allow for the effective dissolution of other substances, facilitating various manufacturing and chemical reaction procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 19781-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19781-29:
(7*1)+(6*9)+(5*7)+(4*8)+(3*1)+(2*2)+(1*9)=144
144 % 10 = 4
So 19781-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-4-7-8-10(11)9(5-2)6-3/h9H,4-8H2,1-3H3
19781-29-4Relevant articles and documents
Cerium(III) chloride remarkably increases the rates of formation and yields of ketones in the reaction of lithium carboxylates with organolithiums
Ahn, Yoonmo,Cohen, Theodore
, p. 203 - 206 (2007/10/02)
The presence of CeCl3 greatly increases the yield of ketones in the reaction of organolithiums with lithium carboxylates. The CE(III) suppresses the enolization of the lithium carboxylate, previously unrecognized as a competing reaction except in special cases, and the formation of tertiary alcohols. One of the reasons for the latter effect is a surprising increase in the rate of addition of the organometallic to the lithium carboxylate in the presence of Ce(III).
