871482-85-8 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Cyclohexylmethyl-2-hydroxycyclopent-2-enone is used as an intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 3-Cyclohexylmethyl-2-hydroxycyclopent-2-enone is used as a building block in the creation of various agrochemicals, potentially enhancing crop protection and yield.
Used as a Flavoring Agent:
3-Cyclohexylmethyl-2-hydroxycyclopent-2-enone is utilized as a flavoring agent, capitalizing on its unique properties to impart specific tastes in food products.
Used in Cosmetic Formulations:
3-CYCLOHEXYLMETHYL-2-HYDROXYCYCLOPENT-2-ENONE is also used as a component in cosmetic products, where it may contribute to the product's efficacy, texture, or scent.
Used in Fragrance Development:
3-Cyclohexylmethyl-2-hydroxycyclopent-2-enone is employed in the development of fragrances, leveraging its chemical structure to create distinct and appealing scents for various applications.
For further research and development:
Due to its potential biological activities or properties, 3-Cyclohexylmethyl-2-hydroxycyclopent-2-enone may be of interest for additional research and development, possibly leading to new applications and uses across different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 871482-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,4,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 871482-85:
(8*8)+(7*7)+(6*1)+(5*4)+(4*8)+(3*2)+(2*8)+(1*5)=198
198 % 10 = 8
So 871482-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c13-11-7-6-10(12(11)14)8-9-4-2-1-3-5-9/h9,14H,1-8H2
871482-85-8Relevant academic research and scientific papers
Gao, Fuye,Burnell, D. Jean
, p. 356 - 359 (2006)
Lewis acid-mediated reactions of 1,2-bis(trimethylsilyloxy)-cyclobutene with acetals derived from a variety of aldehydes, followed by treatment with Amberlyst 15 resin in TFA, yielded 1,3-cyclopentanedione products, but reactions with 3,3-dimethyl-1,2-bis(trimethylsilyloxy)cyclobutene led to 1,2-cyclopentanediones. Reactions of 1,2-bis(trimethylsilyloxy)-cyclopentene gave intermediates that did not undergo skeletal rearrangement with Amberlyst 15 resin in TFA.
