115315-95-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 1-phenyl-1H-pyrazole-3-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of biologically active molecules. Its presence in the synthesis process aids in creating compounds with potential therapeutic effects.
Used in Agrochemical Development:
In the agrochemical industry, ethyl 1-phenyl-1H-pyrazole-3-carboxylate serves as a crucial component in the creation of pesticides and other agrochemicals, leveraging its reactivity and structural properties to enhance the effectiveness of these products.
Used in Novel Materials Development:
Ethyl 1-phenyl-1H-pyrazole-3-carboxylate is utilized as a chemical precursor in the development of novel materials, where its unique properties can be harnessed to produce new materials with specific characteristics for various applications.
Used in Chemical Research and Development:
As a reagent in chemical research and development, ethyl 1-phenyl-1H-pyrazole-3-carboxylate is employed to explore new chemical reactions and mechanisms, potentially leading to the discovery of new compounds and processes that can be applied across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 115315-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,1 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115315-95:
(8*1)+(7*1)+(6*5)+(5*3)+(4*1)+(3*5)+(2*9)+(1*5)=102
102 % 10 = 2
So 115315-95-2 is a valid CAS Registry Number.
115315-95-2Relevant academic research and scientific papers
Martins, Marcos A. P.,Freitag, Rogerio A.,Da Rosa, Adriano,Flores, Alex F. C.,Zanatta, Nilo,Bonacorso, Helio G.
, p. 217 - 220 (1999)
A one-pot synthesis of 1-methyl- and 1-phenylpyrazole-3(5)-ethyl esters 2,3a-e by the cyclocondensation of β-alkoxyvinyl trichloromethyl ketones 1a- e with methyl and phenyl hydrazine hydrochloride under mild conditions, is reported. A study using compounds la-e with different substituents proved that these are versatile building blocks for the synthesis of pyrazole derivatives, having a 3(5)-ethoxycarbonyl substituent in good yields (60- 89%). The hydrazine and β-alkoxyvinyl trichloromethyl ketone substituent effects on the reaction regiochemistry on the formation of the 1,3- and 1,5- isomer were observed.
Shimizu,Hayashi,Nishio,Teramura
, p. 787 - 790 (1984)
C-Ethoxycarbonylnitrilimines treated with monosubstituted olefins predominantly gave 5-substituted 3-ethoxycarbonyl-2-pyrazolines. From the analysis of the relative rate and regioselectivity of a variety of monosubstituted olefins for the cycloaddition, t
