886361-78-0 Usage
Member of the pyridine family
This compound belongs to a family of chemical compounds that share a similar structure, specifically a six-membered ring with nitrogen atoms.
Fluorine and nitro group attached to a phenyl ring
The compound has a phenyl ring with a fluorine atom and a nitro group (-NO2) attached to it, which gives it unique chemical properties.
Used in research and pharmaceutical applications
2-(4-FLUOROPHENYL)-5-NITROPYRIDINE is commonly used in scientific research and in the development of new drugs.
Precursor in chemical synthesis
This compound can be used as a starting material in the synthesis of other chemical compounds.
Potential uses in agrochemicals and organic materials
Due to its unique chemical properties, 2-(4-FLUOROPHENYL)-5-NITROPYRIDINE may have potential applications in the fields of agriculture and organic materials.
Proper safety precautions and regulations
Like many chemicals, it is important to handle and use 2-(4-FLUOROPHENYL)-5-NITROPYRIDINE according to proper safety guidelines and regulations to prevent harm to people and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 886361-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 886361-78:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*1)+(2*7)+(1*8)=220
220 % 10 = 0
So 886361-78-0 is a valid CAS Registry Number.
886361-78-0Relevant articles and documents
A Zwitterionic Palladium(II) Complex as a Precatalyst for Neat-Water-Mediated Cross-Coupling Reactions of Heteroaryl, Benzyl, and Aryl Acid Chlorides with Organoboron Reagents
Ramakrishna, Visannagari,Rani, Morla Jhansi,Reddy, Nareddula Dastagiri
, p. 7238 - 7255 (2018/01/01)
The Suzuki–Miyaura cross-coupling (SMC) reactions of several heteroaryl chlorides, benzyl chlorides, and aryl acid chlorides with (hetero)arylboron reagents have been investigated in the presence of [Pd(HL1)(PPh3)Cl2] (I) [HL1 = 3-[(2,6-diisopropylphenyl)-1-imidazolio]-2-quinoxalinide] as catalyst and K2CO3 as base in neat water. The synthesis of the heterocycle-containing biaryls required the addition of 2 mol-% of a phosphine ligand (PPh3 or X-Phos). A combination of more than 115 substrates were screened and it was found that I is a versatile catalyst that can produce heterocycle-containing biaryls, diarylmethanes, and benzophenones in moderate-to-excellent yields.
Cross-coupling study of iodo/chloropyridines and 2-chloroquinoline with atom-economic triarylbismuth reagents under Pd-catalysis
Rao, Maddali L.N.,Dhanorkar, Ritesh J.
, p. 338 - 349 (2015/03/04)
This study describes the palladium-catalyzed couplings of iodopyridines, chloropyridines, and chloroquinoline with atom-economic BiAr3 reagents in sub-stoichiometric loadings. Mono-arylations of iodo and chloropyridines produced arylpyridines i
