120982-59-4 Usage
Chemical group
Pyrazole group
Structural feature
Contains a pyrazol-1-yl moiety substituted with two phenyl groups
Functional group
Amide functional group
Additional substituent
Diethylaminopropyl substituent
Potential applications
Pharmaceutical applications
Central nervous system modulation
Ability to modulate the central nervous system
Anti-inflammatory properties
Reported anti-inflammatory properties
Analgesic properties
Reported analgesic properties
Neuromuscular blocking agent
Potential use as a neuromuscular blocking agent due to the diethylaminopropyl group
Research and development
Synthesis and characterization may provide valuable insights for further research and development in the field of medicinal chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 120982-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,8 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120982-59:
(8*1)+(7*2)+(6*0)+(5*9)+(4*8)+(3*2)+(2*5)+(1*9)=124
124 % 10 = 4
So 120982-59-4 is a valid CAS Registry Number.
120982-59-4Relevant articles and documents
1H-pyrazole-1-alkanamines antiarrhythmic compositions and use
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, (2008/06/13)
N-[alkylamino)alkyl]-3,4(or 4,5)-diaryl-1H-pyrazole-1-(branched)alkanamides and pyrazole-1-alkanamines useful for treating cardiac arrhythmias in mammals, are prepared by reacting a lower-alkyl ester of pyrazole-1-acetic acid with an appropriate diamine followed by reduction or by reacting the anion of a lower-alkyl ester of a pyrazole-1-acetic acid with an alkylating agent followed by displacement of the ester by an appropriate amine.
1H-pyrazole-1-alkanamides, antiarrhythmic compositions and use
-
, (2008/06/13)
N-[(disubstituted amino)alkyl]-3,4 (or 4,5)-diaryl-1H-pyrazole-1-acetamides and pyrazole-1-propanamides, useful for treating cardiac arrhythmias in mammals, are prepared by reacting a lower-alkyl ester of pyrazole-1-acetic or propanoic acid with an appropriate diamine or by reacting a lower-alkyl ester of a pyrazole-1-acetic or propanoic acid with an ω-aminoalkanol, followed by activation of the alcohol and displacement by an appropriate amine.
