129521-39-7 Usage
Derivative of 1,2,4-triazole
A heterocyclic compound based on the 1,2,4-triazole structure, which consists of a 5-membered ring containing three nitrogen atoms and two carbon atoms.
Methylsulfonyl group
A functional group (-SO2CH3) attached to the fifth carbon of the 1,2,4-triazole core, which contributes to the compound's chemical properties and reactivity.
Phenyl group
A benzene ring (C6H5) attached to the third carbon of the 1,2,4-triazole core, which influences the compound's stability and chemical behavior.
Pharmaceutical intermediate
The compound can be used as a building block in the synthesis of pharmaceuticals.
Building block in organic synthesis
It can be employed as a precursor in the preparation of other organic compounds.
Potential pesticide
The compound may exhibit pesticidal properties and can be used to control pests in agriculture.
Biological activity
Although not extensively studied, the compound may possess biological activity that could be relevant in various applications.
Safety and handling
Proper handling and storage procedures should be followed to ensure the safe use and management of the compound, as with any chemical substance.
Check Digit Verification of cas no
The CAS Registry Mumber 129521-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,2 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129521-39:
(8*1)+(7*2)+(6*9)+(5*5)+(4*2)+(3*1)+(2*3)+(1*9)=127
127 % 10 = 7
So 129521-39-7 is a valid CAS Registry Number.
129521-39-7Relevant articles and documents
5-Aryl-3-(alkylthio)-4H-1,2,4-triazoles as selective antagonists of strychnine-induced convulsions and potential antispastic agents
Kane,Staeger,Dalton,Miller,Dudley,Ogden,Kehne,Ketteler,McCloskey,Senyah,Chmielewski,Miller
, p. 125 - 132 (2007/10/02)
Selected examples from three series of isomeric (alkylthio)-1,2,4- triazoles were prepared and examined for anticonvulsant activity versus strychnine-, maximal-electroshock-, pentylenetetrazole-, and 3- mercaptopropionic-acid-induced seizures in mice. A n
