112960-08-4 Usage
Molecular weight
284.13 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Pyrazole-4-carboxylic acid derivative The compound is a derivative of 1H-Pyrazole-4-carboxylic acid, which is a five-membered heterocyclic ring system containing one nitrogen atom and one oxygen atom.
Ethyl ester
The compound is an ethyl ester, meaning it has an ethoxycarbonyl group (-COOEt) attached to the pyrazole ring.
Amino group
The compound contains an amino group (-NH2), which is a nitrogen atom bonded to two hydrogen atoms.
Dichlorophenyl group
The compound has a 3,5-dichlorophenyl group, which is a phenyl ring with two chlorine atoms attached at the 3rd and 5th positions.
Applications
Medicinal chemistry and pharmaceutical development The compound has potential applications in the field of medicinal chemistry, particularly in the development of novel drugs and therapeutics.
Unique structure and properties
The compound's unique structure and properties make it a valuable tool for studying biological processes and designing new drug candidates.
Commonly used in chemical research
The compound is frequently used in chemical research to study its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 112960-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,6 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112960-08:
(8*1)+(7*1)+(6*2)+(5*9)+(4*6)+(3*0)+(2*0)+(1*8)=104
104 % 10 = 4
So 112960-08-4 is a valid CAS Registry Number.
112960-08-4Relevant academic research and scientific papers
Luebbers, Thomas,Angehrn, Peter,Gmuender, Hans,Herzig, Silvia,Kulhanek, Josef
, p. 821 - 826 (2000)
We report herein the design and synthesis of ATP-analogues, namely 4-amino-pyrazolo[3,4-d]pyrimidines and 4-amino-pyrazolo[1,5-a][1,3,5]triazines, with DNA gyrase inhibitory activity. Among these series, some compounds exhibited promising antibacterial activity. (C) 2000 Elsevier Science Ltd. All rights reserved.
Synthesis of pyrazole-carboxamides and pyrazole-carboxylic acids derivatives: Simple methods to access powerful building blocks
Ferreira, Byanca Silva,Silva, Rafaela Corrêa,Souto, Bernardo Araújo,Dos Santos, Maurício Silva
, p. 335 - 343 (2021/09/07)
Hybrid systems containing pyrazole moiety show a wide spectrum of biological activities. To access novel hybrids with pyrazole ring, in this work we synthesized twenty pyrazole-carboxylic acids and twenty pyrazole-carboxamides, using simple synthetic methods, to be used as building blocks in the development of new structures.
A New Synthesis of 1-Aryl-5-cyano-1H-pyrazole-4-carboxylic Acid, Ethyl Esters
Beck, James R.,Ackmann, Stephen A.,Staszak, Michael A.,Wright, Fred L.
, p. 955 - 958 (2007/10/02)
A novel conversion of 5-amino-1-aryl-1H-pyrazole-4-carboxylic acid, ethyl esters to the corresponding 5-cyano esters is described.The process involves nonaqueous diazotation of the amine to form the methyl thioether, which is oxidized to the methyl sulfon
