95656-60-3 Usage
Uses
Used in Pharmaceutical Development:
1-(4'-Amino-3'-chloro-5'-fluoro-phenyl)-2-cyclopropylamino-ethanol is used as a chemical compound in the pharmaceutical industry for the development of drugs. Its unique structure with various substituents on the phenyl ring indicates that it may have specific receptor interactions, which could be harnessed for therapeutic purposes.
Used in Research and Development:
In the field of chemical and biological research, 1-(4'-Amino-3'-chloro-5'-fluoro-phenyl)-2-cyclopropylamino-ethanol serves as a valuable compound for studying its potential biological activities and interactions with various receptors. This research could lead to the discovery of new drugs or therapeutic agents.
Used in Drug Design and Synthesis:
1-(4'-Amino-3'-chloro-5'-fluoro-phenyl)-2-cyclopropylamino-ethanol is used as a building block or starting material in the design and synthesis of new drugs. Its unique functional groups and structural features can be exploited to create novel pharmaceutical compounds with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4'-Amino-3'-chloro-5'-fluoro-phenyl)-2-cyclopropylamino-ethanol is utilized as a compound for studying its potential as a therapeutic agent. Its pharmacological properties and interactions with biological targets can provide insights into the development of new drugs for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 95656-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95656-60:
(7*9)+(6*5)+(5*6)+(4*5)+(3*6)+(2*6)+(1*0)=173
173 % 10 = 3
So 95656-60-3 is a valid CAS Registry Number.
95656-60-3Relevant 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.
BRONCHOSPASMOLYTIC 1-(P-AMINO-PHENYL)-2-AMINO-ETHANOLS-(1) AND SALTS
-
, (2008/06/13)
Racemic and optically active compounds of the formula wherein R1 is hydrogen, fluorine, chlorine, bromine, iodine or cyano, R2 is fluorine, trifluoromethyl, nitro or cyano, and R3 is alkyl of 3 to 5 carbon atoms, hydroxy(alkyl of 3 to 5 carbon atoms), cycloalkyl of 3 to 5 carbon atoms, 1-(3,4-methylenedioxy-phenyl)-2-propyl or 1-(p-hydroxy-phenyl)-2-propyl, and non-toxic, pharmacologically acceptable acid addition salts thereof; the compounds as well as their salts are useful as analgesics, uterospasmolytics, bronchospasmolytics and antispastics for the skeletal musculature, and especially as beta 2-receptor mimetics and beta 1-receptor blockers
