517870-26-7 Usage
Uses
Used in Organic Synthesis:
5-(3-Methoxy-phenyl)-2H-pyrazole-3-carboxylic acid methyl ester is used as a synthetic intermediate for the creation of various organic compounds. Its versatile structure allows for the development of new molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-(3-Methoxy-phenyl)-2H-pyrazole-3-carboxylic acid methyl ester is used as a key component in the design and synthesis of new drugs. Its pyrazole ring and functional groups can be modified to create bioactive molecules with therapeutic properties.
Used in Drug Development:
5-(3-Methoxy-phenyl)-2H-pyrazole-3-carboxylic acid methyl ester is employed as a building block in the development of novel pharmaceuticals. Its unique structure and reactivity make it a valuable asset in the creation of drugs with improved efficacy and selectivity.
Used in Biochemical Research:
In the field of biochemistry, 5-(3-Methoxy-phenyl)-2H-pyrazole-3-carboxylic acid methyl ester is used as a research tool to study the interactions between molecules and biological systems. Its specific properties can provide insights into the mechanisms of various biological processes.
Used in Chemical Industry:
5-(3-Methoxy-phenyl)-2H-pyrazole-3-carboxylic acid methyl ester is utilized in the chemical industry for the production of specialty chemicals and materials. Its unique structure and reactivity contribute to the development of innovative products with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 517870-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,7,8,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 517870-26:
(8*5)+(7*1)+(6*7)+(5*8)+(4*7)+(3*0)+(2*2)+(1*6)=167
167 % 10 = 7
So 517870-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O3/c1-16-9-5-3-4-8(6-9)10-7-11(14-13-10)12(15)17-2/h3-7H,1-2H3,(H,13,14)
517870-26-7Relevant academic research and scientific papers
Intramolecular Cyclization of Vinyldiazoacetates as a Versatile Route to Substituted Pyrazoles
Drikermann, Denis,G?rls, Helmar,Kerndl, Valerie,Vilotijevic, Ivan
, p. 1158 - 1162 (2020/07/20)
Vinyldiazo compounds undergo a thermal electrocyclization to form pyrazoles in yields of up to 95percent. The reactions are operationally simple, use readily available starting materials, require no intervention of a catalyst, and enable the synthesis of mono-, di- A nd tri-substituted pyrazoles. With the ability to produce highly substituted pyrazoles and the flexibility in installing various types of substituents, this method constitutes a new entry to this valuable heterocyclic scaffold and may be of interest to all branches of the chemical industry.
HETEROCYCLIC INHIBITORS OF MCT4
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Paragraph 0569, (2018/06/30)
Disclosed herein are compounds and compositions useful in the treatment of MCT4 mediated diseases, such as proliferative and inflammatory diseases, having the structure of Formula I: Methods of inhibition MCT4 activity in a human or animal subject are also provided.
