671182-58-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-chlorophenyl)-5-methyl-1H-pyrazole is used as a selective inhibitor for [application type] the enzyme FAAH (fatty acid amide hydrolase) for [application reason] its involvement in the metabolism of endocannabinoids. This selective inhibition may have therapeutic implications in various conditions related to the endocannabinoid system.
1-(4-chlorophenyl)-5-methyl-1H-pyrazole is also used as a potential agent for [application type] anti-inflammatory and analgesic properties for [application reason] its ability to modulate the immune response and provide pain relief.
Used in Medicinal Chemistry Research:
1-(4-chlorophenyl)-5-methyl-1H-pyrazole serves as a valuable compound in [application type] medicinal chemistry research for [application reason] its unique structure and functional groups, which can be utilized in the development of new drugs targeting various biological pathways and diseases.
Used in Drug Development:
In the field of drug development, 1-(4-chlorophenyl)-5-methyl-1H-pyrazole is used as a starting point or a structural template for [application type] designing new pharmaceuticals for [application reason] its potential to modulate various biological targets and pathways, leading to the creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 671182-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,1,1,8 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 671182-58:
(8*6)+(7*7)+(6*1)+(5*1)+(4*8)+(3*2)+(2*5)+(1*8)=164
164 % 10 = 4
So 671182-58-4 is a valid CAS Registry Number.
671182-58-4Relevant academic research and scientific papers
Rearrangements of N-heterocyclic carbenes of pyrazole to 4-aminoquinolines and benzoquinolines
Dreger, Andrij,Cisneros Camuna, Rafael,Munster, Niels,Andras Rokob, Tibor,Papai, Imre,Schmidt, Andreas
experimental part, p. 4296 - 4305 (2010/10/19)
1-Phenyl-substituted pyrazolium salts, formed by quaternization of pyrazoles with benzyl halides or long-chain alkyl halides, deprotonate to pyrazol-3-ylidenes that undergo a sequence of ring-opening, ring-closure, and tautomerization to new substituted 4
