97760-74-2 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(4-amino-3-chloro-5-fluorophenyl)is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications. The presence of the amino group enables further functionalization and modification, while the chloro and fluoro substituents can influence the compound's pharmacokinetic and pharmacodynamic properties.
Used in Agrochemical Industry:
Ethanone, 1-(4-amino-3-chloro-5-fluorophenyl)is also utilized in the agrochemical industry for the synthesis of pesticides and other agrochemicals. Its versatile structure allows for the development of compounds with targeted biological activity, such as herbicides, insecticides, and fungicides. The presence of the chloro and fluoro groups can enhance the compound's stability and effectiveness in agricultural applications.
Used in Drug Discovery and Development:
Ethanone, 1-(4-amino-3-chloro-5-fluorophenyl)is employed as a valuable building block in drug discovery and development. Its unique structure and potential biological activity make it an attractive candidate for the design and synthesis of novel therapeutic agents. Researchers can exploit the compound's functional groups to create new molecules with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 97760-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97760-74:
(7*9)+(6*7)+(5*7)+(4*6)+(3*0)+(2*7)+(1*4)=182
182 % 10 = 2
So 97760-74-2 is a valid CAS Registry Number.
97760-74-2Relevant academic research and scientific papers
Synthesis of further amino-halogen-substituted phenyl-aminoethanols
Kruger,Keck,Noll,Pieper
, p. 1612 - 1624 (2007/10/02)
Starting from clenbuterol as a lead structure, new 4-amino-phenyl-aminoethanol analogues have been synthesized by different approaches. In these compounds one or both of the chlorine atoms of clenbuterol are replaced by other residues. This has led to compounds with high intrinsic β2-mimetic and/or β1-blocking activities. 1-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert.-butylamino-ethanol hydrochloride (mabuterol) has been selected for clinical development. A detailed description is also given of the syntheses of new intermediate acetophenone derivatives as well as of the resolution of mabuterol into its enantiomers.
