65419-99-0 Usage
Description
1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]-, also known as dicyclohexylketone, is a chemical compound characterized by its molecular formula C20H22O2. This white crystalline solid exhibits a faint, sweet, citrus-like odor and is recognized for its versatile applications across various industries.
Uses
Used in Fragrance Industry:
1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]is utilized as a fragrance ingredient in the perfume industry due to its pleasant, citrus-like scent. Its unique aroma adds depth and complexity to fragrance formulations, enhancing the overall sensory experience for consumers.
Used in Flavor Industry:
In the food and beverage sector, 1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]serves as a flavoring agent, contributing to the enhancement of taste profiles in various products. Its sweet, citrus-like odor makes it a valuable addition to the flavor palette, providing a distinct and appealing taste sensation.
Used in Chemical Processes:
As a solvent, 1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]plays a crucial role in chemical processes. Its ability to dissolve a wide range of substances makes it an essential component in various industrial applications, facilitating reactions and improving process efficiency.
Used in Organic Synthesis:
In the realm of organic synthesis, 1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]functions as a valuable reagent. Its chemical properties enable it to participate in a variety of reactions, contributing to the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]holds potential in the pharmaceutical industry for the synthesis of various drugs and pharmaceuticals. Its unique chemical structure allows for the development of novel therapeutic agents, potentially leading to advancements in medical treatments.
However, it is important to handle 1(2H)-Naphthalenone, 3,4-dihydro-2-[(2-oxocyclohexyl)phenylmethyl]with caution, as it can be harmful if swallowed, inhaled, or comes into contact with the skin. Additionally, it may have harmful effects on aquatic organisms, necessitating proper safety measures and environmental considerations during its use and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 65419-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,1 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65419-99:
(7*6)+(6*5)+(5*4)+(4*1)+(3*9)+(2*9)+(1*9)=150
150 % 10 = 0
So 65419-99-0 is a valid CAS Registry Number.
65419-99-0Relevant articles and documents
Kinetics and Mechanisms of Nucleophilic Displacements with Heterocycles as Leaving Groups. 2. N-Benzylpyridinium Cations: Rate Variation with Steric Effects in the Leaving Group
Katritzky, Alan R.,El-Mowafy, Azzahra M.,Musumarra, Giuseppe,Sakizadeh, Kumars,Sana-Ullah, Choudhry,et al.
, p. 3823 - 3830 (2007/10/02)
N-Benzyl groups are transferred to piperidine from pyridinium ions by unimolecular SN1 and/or bimolecular SN2 mechanisms.Steric acceleration by α-phenyl groups is reduced by an adjacent β-methyl group but increased by constraining th
