111079-04-0 Usage
Description
3-Trifluoromethyl-5-methyl-1-(phenyl)pyrazole is a pyrazole derivative with the molecular formula C11H9F3N2. It features a trifluoromethyl group, which is highly electronegative and sterically demanding, and a phenyl group, contributing to its potential as a building block for more complex organic molecules. This chemical compound has interesting chemical properties and potential for biological activity, making it a promising candidate for pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research and Drug Development:
3-Trifluoromethyl-5-methyl-1-(phenyl)pyrazole is used as a chemical compound in pharmaceutical research and drug development due to its unique chemical properties and potential for biological activity. Its electronegative trifluoromethyl group and phenyl group may contribute to its interactions with biological targets, offering opportunities for the design of new therapeutic agents.
Used in Organic Synthesis:
3-Trifluoromethyl-5-methyl-1-(phenyl)pyrazole is used as a building block in organic synthesis for the creation of more complex organic molecules. Its structural features can be leveraged to develop new compounds with specific properties and applications in various fields, including materials science and medicinal chemistry.
Further research into the properties and potential uses of 3-trifluoromethyl-5-methyl-1-(phenyl)pyrazole may reveal its utility in additional areas of chemistry and medicine, expanding its applications and significance in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 111079-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,7 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111079-04:
(8*1)+(7*1)+(6*1)+(5*0)+(4*7)+(3*9)+(2*0)+(1*4)=80
80 % 10 = 0
So 111079-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9F3N2/c1-8-7-10(11(12,13)14)15-16(8)9-5-3-2-4-6-9/h2-7H,1H3
111079-04-0Relevant articles and documents
Synthesis of polysubstituted pyrazoles by a platinum-catalyzed sigmatropic rearrangement/cyclization cascade
Wen, Jia-Jie,Tang, Hai-Tao,Xiong, Kai,Ding, Zong-Cang,Zhan, Zhuang-Ping
, p. 5940 - 5943 (2014)
A highly efficient Pt-catalyzed [3,3] sigmatropic rearrangement/cyclization cascade of N-propargylhydrazones is reported. The process provides expedient access to a variety of highly functionalized pyrazoles. The substrate has good substituted group compa
Small molecule library synthesis using segmented flow
Thompson, Christina M.,Poole, Jennifer L.,Cross, Jeffrey L.,Akritopoulou-Zanze, Irini,Djuric, Stevan W.
experimental part, p. 9161 - 9177 (2012/01/03)
Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper
Regioselective synthesis of trifluoromethyl group substituted pyrazole derivatives from 1-aryl-3,4,4,4-tetrafluoro-2-buten-1-ones
Sano, Keisuke,Hara, Shoji
experimental part, p. 349 - 357 (2010/04/27)
Trifluoromethyl group substituted pyrazole derivatives were prepared from hydrazines and 1-aryl-3,4,4,4-tetrafluoro-2-buten-1-ones obtained by the deoxyfluorination of β-diketones. The reaction proceeded regioselectively and 5-aryl-3-trifluoromethyl-1-phe
