1086392-16-6 Usage
Indazole derivative
A compound that is derived from the indazole structure, which is a five-membered aromatic ring containing three nitrogen atoms.
Carbohydrazide functional group
A functional group within the compound that consists of a hydrazide group (-NHNH2) attached to an indazole ring.
Potential medicinal properties
The compound has been studied for its possible use in medicine, such as being an antitubercular agent (for treating tuberculosis).
Potential use as an intermediate in organic synthesis
1H-Indazole-4-carbohydrazide can be used as a starting material or intermediate in the synthesis of other organic compounds, including pharmaceuticals.
Unique structure and properties
The combination of the hydrazide and indazole ring in the compound's structure contributes to its distinctive properties, making it an interesting target for further research and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1086392-16-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,9 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1086392-16:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*9)+(3*2)+(2*1)+(1*6)=166
166 % 10 = 6
So 1086392-16-6 is a valid CAS Registry Number.
1086392-16-6Relevant articles and documents
Synthesis, α-amylase and α-glucosidase inhibition and molecular docking studies of indazole derivatives
Abubshait, Samar A.,Ahmad, Tauqir,Chigurupati, Sridevi,Chinnam, Sampath,Hisaindee, Soleiman,Nawaz, Muhammad,Qureshi, Faiza,Selvaraj, Manikandan,Shahzad, Sumaira,Taha, Muhammad,Ullah, Nisar
, (2021/08/27)
Herein, we report the synthesis and inhibitory potential of indazole (Methyl 1H-indazole-4-carboxylate) derivatives (1–13) against α-amylase and α-glucosidase enzymes. The described derivatives demonstrated good inhibitory potential with IC50 v
