87629-00-3 Usage
Molecular structure
1H-Pyrazolo[4,3-c]pyridine, 5-acetyl-3-(4-fluorophenyl)-4,5,6,7-tetrahydro-1-(2-phenylethyl)is a complex heterocyclic compound consisting of a pyrazole ring fused to a pyridine ring, with additional acetyl and phenyl groups attached.
Heterocyclic compound
The presence of both pyrazole and pyridine rings makes it a heterocyclic compound, which often have potential pharmaceutical applications due to their presence in bioactive molecules.
Acetyl group
The presence of an acetyl group in the compound makes it a potential pharmacophore, which is a molecular structure responsible for a drug's activity.
Fluorophenyl group
The compound contains a 4-fluorophenyl group, which may contribute to its biological activity and potential pharmaceutical applications.
2-Phenylethyl group
The presence of a 2-phenylethyl group in the compound may also contribute to its biological activity and potential pharmaceutical applications.
Biological activity
The specific structure of the compound suggests it may have biological activity, making it a potential target for drug development or medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 87629-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,2 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87629-00:
(7*8)+(6*7)+(5*6)+(4*2)+(3*9)+(2*0)+(1*0)=163
163 % 10 = 3
So 87629-00-3 is a valid CAS Registry Number.
87629-00-3Relevant academic research and scientific papers
Synthesis, in Vitro 3H>Prazosin Displacement, and in Vivo Activity of 3-Aryl-4,5,6,7-tetrahydropyrazolopyridines, a New Class of Antihypertensive Agents
Winters, Giorgio,Sala, Alberto,Barone, Domenico,Baldoli, Emiliana
, p. 934 - 940 (2007/10/02)
A series of a new 3-aryl-4,5,6,7-tetrahydropyrazolopyridines was synthesized and screened for in vitro 3H>prazosin displacement activity.The results correlated well with their antihypertensive activity in spontaneous hypertensive rats.
