105-24-8 Usage
Description
1-(2-Cyclopentenyl)-2-propanone, a chemical compound with the molecular formula C9H12O, is a cyclic ketone that features a cyclopentenyl group and a propanone group. It is recognized for its fruity and floral odor, and serves as a versatile building block in organic synthesis. 1-(2-CYCLOPENTENYL)-2-PROPANONE is also known for its potential therapeutic properties in medicinal chemistry, making it a valuable asset in both scientific research and industrial applications.
Uses
Used in Pharmaceutical Industry:
1-(2-Cyclopentenyl)-2-propanone is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new medicinal compounds.
Used in Perfume Industry:
In the perfume industry, 1-(2-Cyclopentenyl)-2-propanone is utilized as a component in creating fragrances due to its distinct fruity and floral scent.
Used in Flavoring Agents:
1-(2-Cyclopentenyl)-2-propanone is employed as a flavoring agent in the food industry, enhancing the taste and aroma of various food products.
Used in Organic Synthesis:
As a versatile building block, 1-(2-Cyclopentenyl)-2-propanone is used in organic synthesis for the creation of a wide range of organic compounds.
Used in Scientific Research:
1-(2-CYCLOPENTENYL)-2-PROPANONE is also used in scientific research for exploring its potential therapeutic properties and applications in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 105-24-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105-24:
(5*1)+(4*0)+(3*5)+(2*2)+(1*4)=28
28 % 10 = 8
So 105-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-7(9)6-8-4-2-3-5-8/h2,4,8H,3,5-6H2,1H3
105-24-8Relevant articles and documents
Stereoselective synthesis of ptilocaulin and its 7-epimer
Hassner, Alfred,Murthy, K.S.Keshava
, p. 1407 - 1410 (1986)
A versatile stereoselective synthesis of ptilocaulin 1 and its 7-epimer 22, involving formation of the B-ring by intramolecular nitrile oxide cyclization, is described.
Fragrant mixtures containing esters and ketones
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Page/Page column 38, (2021/01/25)
The invention relates to fragrant mixtures comprising at least one compound of general formula (I), a method for producing claimed fragrant mixtures, particularly perfume oils, perfumed products containing the claimed fragrant mixture, and the use of the compound of general formula (I) to strengthen the natural freshness and/or emanation and/or to mask or reduce greasy and/or metallic notes of one or more fragrant substances that differ from the compound of formula (I).
Asymmetric allylic alkylation of ketone enolates: An asymmetric claisen surrogate
Burger, Erin C.,Tunge, Jon A.
, p. 4113 - 4115 (2007/10/03)
(Chemical Equation Presented) The combination of catalytic palladium(0) and Trost ligand provides an effective catalyst for the rearrangement of allyl β-ketoesters. The mechanism of the transformation involves formation of π-allyl palladium intermediates which undergo enantioselective attack by ketone enolates. Decarboxylation of β-ketocarboxylates allows regiospecific generation of enolates under extremely mild conditions.
Ketone-directed peracid epoxidation of cyclic alkenes
Armstrong, Alan,Barsanti, Paul A.,Clarke, Paul A.,Wood, Anthony
, p. 1373 - 1380 (2007/10/03)
Ketone carbonyl groups are shown to direct the peracid epoxidation of cyclic alkenes with greater selectivity than that displayed by esters. An 18O labelling study is used to show that a dioxirane intermediate is not involved in these reactions.
