5204-27-3 Usage
Chemical structure
1H-Pyrazole, 3-(4-chlorophenyl)-4,5-dihydro-1-phenyl-5-(2-thienyl)is composed of a pyrazole ring, a chlorophenyl group, a phenyl group, and a thienyl group.
Type of compound
It is a heterocyclic compound, meaning it contains a ring of atoms with at least one atom not being carbon.
Potential pharmaceutical applications
Due to its unique structure and properties, this chemical compound may have biological activities of interest to researchers and could potentially be used in the development of new drugs or other medical applications.
Need for further research
More research is needed to fully understand the potential uses and effects of 1H-Pyrazole, 3-(4-chlorophenyl)-4,5-dihydro-1-phenyl-5-(2-thienyl)-, as its biological activities and specific applications are not yet well-established.
Check Digit Verification of cas no
The CAS Registry Mumber 5204-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5204-27:
(6*5)+(5*2)+(4*0)+(3*4)+(2*2)+(1*7)=63
63 % 10 = 3
So 5204-27-3 is a valid CAS Registry Number.
5204-27-3Relevant academic research and scientific papers
Iodine-mediated synthesis of 2-arylbenzoxazoles, 2-arylbenzimidazoles, and 1,3,5-trisubstituted pyrazoles
Ponnala, Shashikanth,Prasad Sahu, Devi
, p. 2189 - 2194 (2007/10/03)
2-Arylbenzoxazoles and 2-arylbenzimidazoles were synthesized by the reaction of aldehydes with 2-aminophenol and O-phenylenediamines in the presence of iodine. 1,3,5-Trisubstituted pyrazoles were synthesized from chalcones and hydrazines in the presence o
Heterocycles. 3. Synthesis and Spectral Data of Some 2-Pyrazolines
El-Rayyes, Nizar R.,Hovakeemian, George H.,Hmoud, Hayat S.
, p. 225 - 229 (2007/10/02)
The reaction of 1,3-diaryl-2-propen-1-ones (Ia-o) with hydrazine and methyl- and phenylhydrazine produced different substituted 2-pyrazolines (III).The structures of these products were evident from their chemical and spectroscopic analysis.
