118718-59-5 Usage
Description
1-(4-Methoxyphenyl)-1H-pyrazole-4-carbonitrile, also known as 4-methoxyphenylpyrazole-4-carbonitrile, is a pyrazole derivative with the molecular formula C11H8N4O. It is a chemical compound that contains a carbonitrile group and features a methoxyphenyl group, which can influence its chemical and biological properties. 1-(4-Methoxyphenyl)-1H-pyrazole-4-carbonitrile is commonly used in the synthesis of pharmaceuticals and agrochemicals and has potential biological and pharmacological activities, such as being an analgesic and anti-inflammatory agent. It is important for research and development in both the pharmaceutical and agricultural industries.
Uses
Used in Pharmaceutical Industry:
1-(4-Methoxyphenyl)-1H-pyrazole-4-carbonitrile is used as an intermediate in the synthesis of pharmaceuticals for its potential biological and pharmacological activities. It serves as a key component in the development of drugs with analgesic and anti-inflammatory properties, contributing to the treatment of various conditions that require pain relief and inflammation control.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(4-Methoxyphenyl)-1H-pyrazole-4-carbonitrile is utilized as a building block in the creation of agrochemicals. Its unique structure and properties make it a valuable component in the development of pesticides, herbicides, and other agricultural chemicals that help improve crop yields and protect plants from pests and diseases.
Used in Research and Development:
1-(4-Methoxyphenyl)-1H-pyrazole-4-carbonitrile plays a significant role in research and development within the pharmaceutical and agricultural sectors. Its potential biological activities and unique chemical structure make it an important compound for exploring new drug candidates and agrochemical products. Researchers use this compound to investigate its properties and evaluate its efficacy in various applications, driving innovation and advancement in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 118718-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,1 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118718-59:
(8*1)+(7*1)+(6*8)+(5*7)+(4*1)+(3*8)+(2*5)+(1*9)=145
145 % 10 = 5
So 118718-59-5 is a valid CAS Registry Number.
118718-59-5Relevant articles and documents
Synthesis of pyrazole-carboxamides and pyrazole-carboxylic acids derivatives: Simple methods to access powerful building blocks
Dos Santos, Maurício Silva,Ferreira, Byanca Silva,Silva, Rafaela Corrêa,Souto, Bernardo Araújo
, 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.
An efficient synthesis of new 5-(1-Aryl-1H-pyrazole-4-yl)-1H-tetrazoles from 1-Aryl-1H-pyrazole-4-carbonitriles via [3 + 2] cycloaddition reaction
Dos Santos, Mauricio S.,Bernardino, Alice M. R.,Pinheiro, Luiz C. S.,Canto-Cavalheiro, Marilene M.,Leon, Leonor L.
, p. 1425 - 1428 (2013/02/23)
A series of new 5-(1-aryl-1H-pyrazole-4-yl)-1H-tetrazoles 4a-l were synthesized via [3 + 2] cycloaddition reaction from 1-aryl-1H-pyrazole-4- carbonitriles 3a-l, sodium azide and ammonium chloride, using dimethylformamide (DMF) as solvent, in good yields: 64-85%. The structures of these newly synthesized compounds were determined from the IR, 1H- and 13C-NMR spectroscopic data and elemental analyses.
New application of heterocyclic diazonium salts. Synthesis of pyrazolo[3,4-d][1,2,3]triazin-4-ones and imidazo[4,5-d][1,2,3]triazin-4-ones
Colomer, Juan Pablo,Moyano, Elizabeth Laura
, p. 1561 - 1565 (2011/05/05)
The pyrazolo[3,4-d][1,2,3]triazin-4-ones 3 and imidazo[4,5-d][1,2,3] triazin-4-ones 4 are analogs structurally related to purines that have showed a wide and significant variety of biological activity. These compounds were synthesized by one-pot diazotization of 5-amino-1H-pyrazole-4-carbonitriles 1 and 5-amino-1H-imidazole-4-carbonitriles 2, respectively.
