56079-16-4 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate is used as a building block for the synthesis of various bioactive compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Antimicrobial Applications:
Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate is used as an antimicrobial agent, demonstrating potential in combating various types of infections caused by bacteria and other microorganisms.
Used in Therapeutic Applications:
Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate is being investigated for its potential as a therapeutic agent for various diseases, offering new avenues for treatment and management of different health conditions.
Used in Agrochemical Industry:
Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate may have applications in the field of agrochemicals, potentially contributing to the development of new pesticides, herbicides, or other agricultural chemicals to improve crop protection and yield.
Used in Materials Science:
Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate may also have potential applications in materials science, where its unique properties could be utilized in the development of new materials with specific characteristics and functions.
Safety Measures:
Due to its moderate toxicity, Ethyl 1,3,5-trimethyl-1H-pyrazole-4-carboxylate should be handled and used with appropriate safety measures, including the use of personal protective equipment, proper storage, and disposal methods to minimize potential risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 56079-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56079-16:
(7*5)+(6*6)+(5*0)+(4*7)+(3*9)+(2*1)+(1*6)=134
134 % 10 = 4
So 56079-16-4 is a valid CAS Registry Number.
56079-16-4Relevant academic research and scientific papers
Toward Continuous-Flow Synthesis of Biologically Interesting Pyrazole Derivatives
Das, Amrita,Ishitani, Haruro,Kobayashi, Shū
supporting information, p. 5127 - 5132 (2019/11/13)
A two-step continuous-flow synthesis of substituted pyrazole derivatives has been developed via the formation of vinylidene keto esters as key intermediates. Heterogeneous Ni2+-montmorillonite was found to be an efficient catalyst for orthoester condensation of 1,3-dicarbonyls under flow conditions. The intermediate reacted with methylhydrazine to afford pyrazole derivatives, for which suitable selection of a solvent played a key role in achieving high yields and excellent regioselectivities of the desired products. An application of this protocol has been demonstrated by the synthesis of a key intermediate for biologically active pyrazoles such as Bixafen. (Figure presented.).
THERMOLYSE DE N,N-DIMETHYL HYDRAZINOPROPENOATES. PREPARATION D'YLURES D'OXOPYRAZOLINIUM ET DE PYRAZOLINONES-5
Coqueret, X.,Bourelle-Wargnier, F.,Chuche, J.
, p. 2263 - 2274 (2007/10/02)
Synthesis and gas phase pyrolysis of various N,N dialkylenhydrazinopropenoate derivatives 7a-g are described.At temperatures above 400 deg C, these compounds give 2-pyrazolin-5 ones 4a-e.At lower temperatures, the pyrazolinium ylides 3a-g are isolated in
