607391-63-9 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(4-chlorophenyl)pentan-2-one is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications with potential therapeutic applications.
Used in the Production of Designer Drugs:
Although it is classified as a controlled substance in some countries due to its potential for misuse and abuse, 1-(4-chlorophenyl)pentan-2-one is also utilized in the production of designer drugs, which are synthetic drugs designed to mimic the effects of controlled substances.
Used in Central Nervous System Modulation:
1-(4-chlorophenyl)pentan-2-one is used as a modulator for the central nervous system, specifically targeting GABA receptors to produce its sedative and anxiolytic effects. This application type is valuable for the development of treatments for anxiety and sleep disorders.
Used in Research and Development:
As a chemical compound with psychoactive properties, 1-(4-chlorophenyl)pentan-2-one is used in research and development to better understand the mechanisms of action and pharmacological effects of similar compounds, which can lead to the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 607391-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,9 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 607391-63:
(8*6)+(7*0)+(6*7)+(5*3)+(4*9)+(3*1)+(2*6)+(1*3)=159
159 % 10 = 9
So 607391-63-9 is a valid CAS Registry Number.
607391-63-9Relevant academic research and scientific papers
AuCl3/AgSbF6-catalyzed rapid epoxide to carbonyl rearrangement
Gudla, Vanajakshi,Balamurugan, Rengarajan
, p. 5243 - 5247 (2012/11/07)
An efficient epoxide to carbonyl rearrangement using catalytic AuCl 3/AgSbF6 has been presented. The reactions are fast and high yielding. β-Hydrogen migration takes place exclusively when hydrogen and methyl or substituted methyl groups are present at β-carbon of epoxide. When phenyl/acetyl/benzoyl and hydrogen are available at same carbon atom, migration of the former is preferred over the latter.
Formation of a Novel Acyl Anion Equivalent by the Electroreduction of Oxazolinium Salts
Shono, Tatsuya,Kashimura, Shigenori,Yamaguchi, Yoshihide,Ishige, Osamu,Uyama, Hiroshi,Kuwata, Fumitaka
, p. 1511 - 1512 (2007/10/02)
Electroreduction of oxazolinium salts synthesized from the corresponding carboxylic acids gave a novel acyl anion equivalent (AAE).The reaction of these AAEs with electrophiles afforded the corresponding aldehydes or ketones in good yields.
