49633-25-2 Usage
Uses
Used in Automotive and Aviation Industries:
3-(1-methylethyl)-pyrazole is used as a fuel additive for its role as a lead scavenger in gasoline. It helps prevent engine knocking and contributes to the reduction of toxic emissions, thereby enhancing the performance and environmental friendliness of engines.
Used in Industrial Applications:
In the industrial sector, 3-(1-methylethyl)-pyrazole serves as a corrosion inhibitor. It protects metal surfaces from degradation caused by exposure to aggressive environments, ensuring the longevity and integrity of metal components in various settings.
Used in Pharmaceutical Research:
3-(1-methylethyl)-pyrazole is also being explored for its potential pharmacological properties. It is studied for its role as an enzyme inhibitor, which could have implications for the development of new pharmaceuticals targeting specific biological pathways.
3-(1-methylethyl)-pyrazole's diverse applications highlight its importance in different fields, from improving fuel efficiency and reducing emissions in transportation to protecting metal surfaces in industrial settings and potentially contributing to advancements in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 49633-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49633-25:
(7*4)+(6*9)+(5*6)+(4*3)+(3*3)+(2*2)+(1*5)=142
142 % 10 = 2
So 49633-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2/c1-5(2)6-3-4-7-8-6/h3-5H,1-2H3,(H,7,8)
49633-25-2Relevant academic research and scientific papers
A NEW SYNTHESIS OF 3,5-DISUBSTITUTED PYRAZOLES BY REACTION OF α,γ-DIPYROLIDINYLGLUTARONITRILES (MASKED α,γ-DIKETONE EQUIVALENTS) WITH HYDRAZINES
Takahashi, Kazumasa,Suzuki, Akira,Ogura, Katsuyuki,Iida, Hirotada
, p. 1075 - 1078 (2007/10/02)
An efficient sequence proposed for a new synthetic method of 3,5-disubstituted pyrazoles involves the reaction of α,γ-dipyrolidinylglutaronitriles (masked α,γ-diketone equivalents) with hydrazines.
