202191-12-6 Usage
Description
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is a chemical compound that is 97% pure and is a derivative of quinoline, a heterocyclic aromatic organic compound. It contains a quinoline ring with a 2-oxazolyl group attached to it. The high purity of this compound makes it suitable for various research and industrial applications.
Uses
Used in Pharmaceutical Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure and properties make it a valuable building block in the development of new pharmaceutical compounds.
Used in Agrochemical Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as an agrochemical intermediate for the development of new pesticides and other agrochemical products. Its high purity and unique structure make it a promising candidate for the creation of effective and environmentally friendly agrochemicals.
Used in Material Science Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a research compound in material science for the development of new materials with unique properties. Its high purity and versatile structure make it a valuable tool for researchers in the field of material science.
Used in Research and Development:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a research compound for further exploration of its potential applications in various fields. Its high purity and unique structure make it an ideal candidate for research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 202191-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,9 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 202191-12:
(8*2)+(7*0)+(6*2)+(5*1)+(4*9)+(3*1)+(2*1)+(1*2)=76
76 % 10 = 6
So 202191-12-6 is a valid CAS Registry Number.
202191-12-6Relevant articles and documents
Concise Total Synthesis of (?)-Vermiculine through a Rhodium-Catalyzed C2-Symmetric Dimerization Strategy
Steib, Philip,Breit, Bernhard
, p. 3532 - 3535 (2019)
A short and efficient synthesis of the C2-symmetric antibiotic (?)-vermiculine by utilizing an enantioselective catalytic one-step dimerization methodology as key-step to construct the core structure is reported. The late-stage modifications feature a double metathesis homologation followed by a double Wacker-type oxidation. These key-steps allowed the synthesis of vermiculine in only seven steps, starting from commercially available building blocks.
Pyridine-oxazoline and quinoline-oxazoline ligated cobalt complexes: Synthesis, characterization, and 1,3-butadiene polymerization behaviors
Guo, Jun,Liu, Heng,Bi, Jifu,Zhang, Chunyu,Zhang, Hexin,Bai, Chenxi,Hu, Yanming,Zhang, Xuequan
, p. 305 - 312 (2015/08/06)
A series of cobalt complexes supported by pyridine-oxazoline (Pyox) and quinoline-oxazoline (Quox) were synthesized. Determined by single crystal X-ray crystallography, complexes 6a and 7c adopted distorted octahedron and trigonal bipyramid geometries, re
Catalyst-controlled Wacker-type oxidation of protected allylic amines
Michel, Brian W.,McCombs, Jessica R.,Winkler, Andrea,Sigman, Matthew S.
supporting information; experimental part, p. 7312 - 7315 (2010/11/05)
On the contrary: Utilizing the [Pd-(quinox)]-TBHP catalyst system, protected allylic amines were oxidized with high selectivity for the methyl ketone product. This is contrary to the results obtained by the substrate-controlled Tsuji-Wacker oxidation, which highlights the catalyst-controlled system presented here (see scheme). A variety of N-pro-tecting groups undergo selective oxidation with high ketone selectivity. TBHP = tert-butylhydroperoxide.