60656-04-4 Usage
Class
Indazoles
Structural feature
Phenyl group attached to the indazole ring structure
Usage
Medicinal chemistry for the development of potential pharmaceutical drugs
Biological activities
Anticancer, antifungal, and antiviral properties
Importance
Promising molecule for further research and development in the pharmaceutical industry due to its unique structure and diverse biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 60656-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60656-04:
(7*6)+(6*0)+(5*6)+(4*5)+(3*6)+(2*0)+(1*4)=114
114 % 10 = 4
So 60656-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H14N2/c1-2-7-15(8-3-1)19-17-14(12-18-19)11-10-13-6-4-5-9-16(13)17/h1-9,12H,10-11H2
60656-04-4Relevant articles and documents
Palladium-catalyzed C-N bond formation: synthesis of 1-aryl-1H-pyrazoles from β-bromovinyl aldehydes and arylhydrazines
Cho, Chan Sik,Patel, Daksha B.
, p. 6388 - 6391 (2007/10/03)
Cyclic and acyclic β-bromovinyl aldehydes are cyclized with an array of arylhydrazines in toluene at 125 °C in the presence of a palladium catalyst and a phosphorus chelating ligand together with NaOtBu to give 1-aryl-1H-pyrazoles in moderate t
The antiarrhythmic and antiinflammatory activity of a series of tricyclic pyrazoles
Hamilton
, p. 545 - 553 (2007/10/04)
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