50920-46-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Ethyl-5-methyl-1H-pyrazole-3-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals due to its potential biological activities and its role as an inhibitor of acetyl-CoA carboxylase enzyme. This makes it a potential target for the development of new drugs for metabolic diseases.
Used in Agrochemical Industry:
1-Ethyl-5-methyl-1H-pyrazole-3-carboxylic acid is used as a building block in the synthesis of agrochemicals, leveraging its potential biological activities for applications in agriculture.
Used in Medicinal Chemistry Research:
As a pyrazole derivative with potential anti-inflammatory and anti-cancer properties, 1-ethyl-5-methyl-1H-pyrazole-3-carboxylic acid is used in medicinal chemistry research for the development of new therapeutic agents.
Used in Drug Development for Metabolic Diseases:
Due to its inhibitory effect on the acetyl-CoA carboxylase enzyme involved in fatty acid synthesis, 1-ethyl-5-methyl-1H-pyrazole-3-carboxylic acid is used in the development of new drugs targeting metabolic diseases.
Overall, 1-ethyl-5-methyl-1H-pyrazole-3-carboxylic acid is a valuable chemical compound with diverse applications in the fields of medicine and agriculture, offering potential benefits in the development of new drugs and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 50920-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,2 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50920-46:
(7*5)+(6*0)+(5*9)+(4*2)+(3*0)+(2*4)+(1*6)=102
102 % 10 = 2
So 50920-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2/c1-3-9-5(2)4-6(8-9)7(10)11/h4H,3H2,1-2H3,(H,10,11)
50920-46-2Relevant academic research and scientific papers
Pyrazole N-alkylation method
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Paragraph 0027; 0028; 0029, (2018/12/14)
The invention provides a pyrazole N-alkylation method. Pyrazole or pyrazole derivatives and alkyl halogenated hydrocarbons react in a solvent under the existence of quaternary ammonium salt catalysts;N-alkyl substituted pyrazole is obtained. The method provided by the invention has the advantages that the operation is simple; the cost is low; the anhydrous oxygen-free environment is not needed; heating is not needed; the yield is high; the amplified industrialized production can be easily realized.
2-(pyrazol-3-yl)carbapenem derivatives
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, (2008/06/13)
Disclosed are 1-, 6- and 2-substituted-1-carba-2-penem-3-carboxylic acids, a process for their preparation, pharmaceutical compositions comprising said compounds and a method of using them to treat bacterial infections.
Pyrazolodiazepines. 1,3 (and 2,3) dialkyl 4,6 dihydro 8 arylpyrazolo[4,3 e][1,4] diazepin 5 ones as antianxiety agents
DeWald,Nordin,L'Italien,Parcell
, p. 1346 - 1354 (2007/10/04)
A series of 1, 3 (and 2, 3) dialkyl 4, 6 dihydro 8 arylpyrazolo [4, 3 e][1, 4] diazepin 5 ones was synthesized and evaluated for psychotropic activity. Intermediates are new dialkylnitropyrazolyl aryl ketones prepared from dialkylnitropyrazolecarboxylic acids. Many of these pyrazolodiazepines exhibit high CNS activity in animals. One compound, 1 ethyl 4, 6 dihydro 3 methyl 8 phenylpyrazolo [4, 3 e] [1, 4] diazepin 5 (1H) one is about as potent as diazepam as an antianxiety agent with less sedative properties and is being studied in the clinic.
