154639-75-5 Usage
Uses
Used in Pharmaceutical Research:
Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)-, is utilized as a research compound in the pharmaceutical industry for its potential applications in drug discovery and development. The combination of the methylamino and sulfinyl groups in its structure makes it a valuable candidate for further investigation in medicinal chemistry.
Used in Drug Discovery:
In the field of drug discovery, Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)-, is employed as a lead compound for the development of new pharmaceutical agents. Its unique chemical properties and potential biological activities offer opportunities for the creation of novel therapeutic agents with improved efficacy and selectivity.
Used in Medicinal Chemistry:
Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)-, is also used in medicinal chemistry as a starting point for the synthesis of new compounds with potential therapeutic applications. The presence of the fluoro-substituted phenyl ring and the methylamino group allows for the exploration of various chemical modifications to optimize the compound's pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 154639-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,6,3 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154639-75:
(8*1)+(7*5)+(6*4)+(5*6)+(4*3)+(3*9)+(2*7)+(1*5)=155
155 % 10 = 5
So 154639-75-5 is a valid CAS Registry Number.
154639-75-5Relevant academic research and scientific papers
Syntheses of Flosequinan: A Novel 4-Quinolone shown to be useful in Congestive Heart Failure
Birch, Alan M.,Davies, Roy V.,Maclean, Lachlan,Robinson, Keith
, p. 387 - 392 (2007/10/02)
Two synthetic routes to flosequinan 1 and flosequinoxan 2 are described in which either ring closure of the β-keto sulfoxides 12 or 13 with ortho esters or cyclisation of the anilinoacrylates 23, 28 or 29 are the key steps.
Process for the preparation of 1-methyl-3-methylthio-4-quinolone and the sulfinyl, and sulfonyl analogs thereof
-
, (2008/06/13)
A process to prepare compounds of formula I STR1 in which n=0, 1 or 2 comprising the cyclisation of compounds of formula II STR2 in which n=0, 1 or 2. The cyclisation may be effected in the presence of an organic or inorganic base or thermally at a temper
