70187-29-0 Usage
Uses
Used in Organic Synthesis:
1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)-, ethyl ester is used as a key intermediate in organic synthesis for the preparation of various chemical compounds. Its unique structure allows for the formation of diverse molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)-, ethyl ester is used as a building block for the development of new drugs. Its potential biological activity makes it a valuable candidate for drug discovery and development, warranting further research into its properties and applications.
Used in Drug Discovery and Development:
Due to its potential biological activity, 1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)-, ethyl ester is of interest in drug discovery and development. It may contribute to the creation of novel pharmaceutical agents with improved therapeutic effects and reduced side effects.
Further research into the properties and potential applications of 1H-Pyrazole-3-carboxylic acid, 4-(4-methoxyphenyl)-, ethyl ester is necessary to fully understand its capabilities and maximize its utility in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 70187-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70187-29:
(7*7)+(6*0)+(5*1)+(4*8)+(3*7)+(2*2)+(1*9)=120
120 % 10 = 0
So 70187-29-0 is a valid CAS Registry Number.
70187-29-0Relevant academic research and scientific papers
1,3-Dipolar cycloaddition of chalcones and arylidene-1,3-dicarbonyls with diazosulfone for the regioselective synthesis of functionalized pyrazoles and pyrazolines
Nair, Deepa,Pavashe, Prashant,Namboothiri, Irishi N.N.
, p. 2716 - 2724 (2018/04/25)
A convenient method for the synthesis of 3-acylpyrazoles and pyrazole-3-carboxylates using diazosulfone as a reactive 1,3-dipole and a diazomethane equivalent is reported here. Chalcones, arylidenemalonates and other arylidene-1,3-dicarbonyls performed we
Efficient method for the synthesis of functionalized pyrazoles by catalyst-free one-pot tandem reaction of nitroalkenes with ethyl diazoacetate
Xie, Jian-Wu,Wang, Zheng,Yang, Wei-Jun,Kong, Li-Chun,Xu, Dong-Cheng
supporting information; experimental part, p. 4352 - 4354 (2009/12/25)
The one-pot synthesis of multisubstituted pyrazole derivatives was achieved via catalyst-free 1,3-dipolar cycloaddition of ethyl diazoacetate and nitroalkenes as the key step and elimination of the leaving group (NO 2 or Br) followed by intramo
