7369-63-3 Usage
Uses
Used in Fragrance Industry:
Ethanone, 1-(1,2,3,4-tetrahydro-1-naphthalenyl)is used as a fragrance ingredient for its aromatic properties, contributing to the creation of perfumes and other scented products.
Used in Food Industry:
In the food industry, Ethanone, 1-(1,2,3,4-tetrahydro-1-naphthalenyl)is used as a flavoring agent, enhancing the taste and aroma of food products.
Used in Pharmaceutical Industry:
Ethanone, 1-(1,2,3,4-tetrahydro-1-naphthalenyl)is used as a starting material in the synthesis of pharmaceuticals, given its potential applications in medicine.
Used in Organic Synthesis:
Ethanone, 1-(1,2,3,4-tetrahydro-1-naphthalenyl)is used as a building block in organic synthesis, allowing for the creation of more complex molecules.
Used in Antimicrobial Applications:
Ethanone, 1-(1,2,3,4-tetrahydro-1-naphthalenyl)is used as an antimicrobial agent for its demonstrated antifungal and antibacterial properties, showing promise in research studies for potential medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7369-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7369-63:
(6*7)+(5*3)+(4*6)+(3*9)+(2*6)+(1*3)=123
123 % 10 = 3
So 7369-63-3 is a valid CAS Registry Number.
7369-63-3Relevant academic research and scientific papers
Bresó-Femenia, Emma,Chaudret, Bruno,Castillón, Sergio
, p. 2741 - 2751 (2015)
Ru nanoparticles stabilised by PPh3 are efficient catalysts for hydrogenation of polycyclic aromatic hydrocarbons (PAHs) containing 2-4 rings under mild reaction conditions. These compounds were partially hydrogenated with good to excellent selectivities just by optimizing the reaction conditions. The influence of the nature of substituents present in different positions of naphthalene on the selectivity of hydrogenation was also studied. Hydrogenation of products containing substituents at position 1 is slower than that of products containing substituents at position 2. In all cases, hydrogenation takes place mainly on the less substituted ring.
