91272-98-9 Usage
Heterocyclic compound
Yes
It contains a ring structure with both carbon and nitrogen atoms.
Pyrrolidinylmethyl group
Attached to the pyrazole ring
A pyrrolidine ring (a saturated, nitrogen-containing ring) is connected to a methyl group, which is then attached to the pyrazole ring.
Pyrazole family
Part of
The compound belongs to the pyrazole family, which is a group of heterocyclic compounds with a five-membered ring containing two nitrogen atoms.
Field of application
Medicinal chemistry and drug discovery
It is commonly used in the development of new drugs and pharmaceuticals.
Pharmacological properties
Cannabinoid receptor ligand
The compound has been explored for its potential activity as a ligand for cannabinoid receptors, which are involved in various physiological processes.
Therapeutic applications
Potential
Studies have shown that 1-(PYRROLIDIN-1-YLMETHYL)-1H-PYRAZOLE may have potential therapeutic applications, making it an interesting target for further research and development in the pharmaceutical industry.
Research and development
Ongoing
The compound is still under investigation for its potential uses and applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 91272-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,7 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91272-98:
(7*9)+(6*1)+(5*2)+(4*7)+(3*2)+(2*9)+(1*8)=139
139 % 10 = 9
So 91272-98-9 is a valid CAS Registry Number.
91272-98-9Relevant academic research and scientific papers
Substituted heterocyclylisoquinolinium salts and compositions and method of use thereof
-
, (2008/06/13)
Substitutued heterocyclylisoquinolinium salts, pharmaceutical compositions containing them and methods for the treatment or prevention of neurodegenerative disorders or neurotoxic injuries utilizing them.
Synthesis of 2-Substituted Imidazoles and Benzimidazoles and of 3-Substituted Pyrazoles by Lithiation of N-(Dialkylamino)methyl Heterocycles
Katritzky, Alan R.,Rewcastle, Gordon W.,Fan, Wei-Qiang
, p. 5685 - 5689 (2007/10/02)
The lithiation of N-(dialkylamino)methyl (aminal) derivatives of imidazole, benzimidazole, and pyrazole (themselves readily available from parent heterocycles, formaldehyde, and a secondary amine) occurs smoothly at 2-, 2-, and 5-positions, respectively, upon treatment with n-butyllithium in ether or tetrahydrofuran.Reaction with electrophiles, and subsequent facile acid-catalyzed hydrolysis of the protecting group, provides 2-substituted imidazoles, 2-substituted benzimidazoles, and 3(5)-substituted pyrazoles in good overall yields.
