484-16-2 Usage
Uses
Used in Pharmaceutical Industry:
9(10H)-Phenanthrenone is used as an intermediate or building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 9(10H)-Phenanthrenone is utilized as a precursor in the production of various agrochemicals. Its role in this industry is crucial for the development of effective pesticides and other agricultural chemicals.
Used in Dye Industry:
9(10H)-Phenanthrenone is used as a building block in the synthesis of dyes, contributing to the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Used in Environmental Research:
Due to its presence as a byproduct of incomplete combustion, 9(10H)-Phenanthrenone is studied in environmental research to understand its impact on air, soil, and sediment quality. This research helps in developing strategies to mitigate its potential environmental and health risks.
Used in Anti-inflammatory and Anticancer Research:
9(10H)-Phenanthrenone has been studied for its potential anti-inflammatory and anticancer properties. Researchers are exploring its therapeutic potential as a treatment for various inflammatory and cancerous conditions, aiming to develop new and effective medications.
Check Digit Verification of cas no
The CAS Registry Mumber 484-16-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 484-16:
(5*4)+(4*8)+(3*4)+(2*1)+(1*6)=72
72 % 10 = 2
So 484-16-2 is a valid CAS Registry Number.
484-16-2Relevant academic research and scientific papers
Laali, Kenneth K.,Herbert, Mark,Cushnyr, Brad,Bhatt, Anand,Terrano, David
, p. 578 - 583 (2001)
The synthetic utility of cerium(IV) triflate Ce(OTf)4 as a reagent for benzylic oxidation has been tested for a variety of aromatic compounds. Insight is provided into various factors that govern these oxidations and their progress. It has been shown that the mode of preparation of Ce(OTf)4 and the % H2O present in the sample have a marked influence on oxidation ability. A variety of mono- and dialkylbenzenes, haloalkylbenzenes, bicyclic and tricyclic ring systems, and alkoxybenzenes have been surveyed. The method offers an easy to perform one-pot reaction for the room temperature synthesis of aromatic ketones and aldehydes from aromatics and has the potential to find wider application.
