137968-14-0 Usage
Derivative of pyrazole
This indicates that the compound is derived from a pyrazole ring, which is a five-membered ring system with two nitrogen atoms.
Contains an amine group
This indicates that the compound contains a nitrogen atom bonded to one hydrogen atom and one alkyl or aryl group.
Phenylmethylene substituent attached to nitrogen
This indicates that a phenyl group (a ring with a double bond) is attached to the nitrogen atom of the amine group through a methylene group (a carbon atom bonded to two hydrogen atoms).
Versatile building block for the preparation of diverse heterocyclic compounds
This suggests that the compound can be used as a starting material for the synthesis of a wide variety of compounds with different ring structures.
Potential biological activities
This suggests that the compound has been studied for its potential effects on living organisms.
Exhibits antimicrobial, antiviral, and anticancer properties
This indicates that the compound has been found to have the ability to inhibit the growth of microorganisms, viruses, and cancer cells, making it a valuable compound for medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 137968-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,6 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137968-14:
(8*1)+(7*3)+(6*7)+(5*9)+(4*6)+(3*8)+(2*1)+(1*4)=170
170 % 10 = 0
So 137968-14-0 is a valid CAS Registry Number.
137968-14-0Relevant academic research and scientific papers
Rearrangement of N-(Alkylamino)azoles in Acid Media: A New Entry to C-Amino-N-substituted Azoles
Salazar, Loreto,Espada, Modesta,Avendano, Carmen,Claramunt, Rosa Maria,Sanz, Dionisia,Elguero, Jose
, p. 1563 - 1567 (2007/10/02)
A ring-opening / ring-closure mechanism for the thermal rearrangement of 1-(alkylamino)pyrazoles into 5-amino-1-alkylpyrazoles in acid medium has been established. 1-(Benzylamino)pyrazoles show a different reactivity, affording bis(5-amino-1-benzyl-4-pyrazolyl)phenylmethanes.The reaction was extended to 1-(alkylamino)indazoles but failed in the case of 1-(alkylamino)-1,2,4-triazoles.
