50966-75-1 Usage
Heterocyclic organic compound
This term refers to a compound that contains a ring structure with at least one nitrogen or other non-carbon atom.
Pyrazine ring
This is a six-membered ring structure with two nitrogen atoms in the 1,4-positions.
Pyrrole ring
This is a five-membered ring structure with one nitrogen atom and is known for its aromatic properties.
Building block for synthesis
2-(1H-pyrrol-1-yl)pyrazine can be used as a starting material for the synthesis of other compounds.
Potential biological activity
2-(1H-pyrrol-1-yl)pyrazine has the potential to interact with biological systems and produce a therapeutic effect.
Precursor for new drugs
2-(1H-pyrrol-1-yl)pyrazine can be used as a starting material for the development of new drugs and therapeutic agents.
Medicinal chemistry and pharmaceuticals applications
2-(1H-pyrrol-1-yl)pyrazine has potential applications in the field of medicinal chemistry and pharmaceuticals due to its unique structure and potential biological activity.
Further research required
More studies and research are needed to fully understand the properties and potential applications of 2-(1H-pyrrol-1-yl)pyrazine.
Check Digit Verification of cas no
The CAS Registry Mumber 50966-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50966-75:
(7*5)+(6*0)+(5*9)+(4*6)+(3*6)+(2*7)+(1*5)=141
141 % 10 = 1
So 50966-75-1 is a valid CAS Registry Number.
50966-75-1Relevant articles and documents
Oxazolidin-2-one as efficient ligand for the copper-catalyzed N- Arylation of pyrrole, imidazole and indole
Ma, Hengchang,Wu, Shang,Sun, Qiangsheng,Lei, Ziqiang
experimental part, p. 212 - 218 (2011/07/07)
Oxazolidin-2-one was found to be a facile ligand for the N-arylation of pyrrole, indole, and imidazole with aryl and heteroaryl iodides, bromides, and chlorides by applying Cul as catalyst. The easy preparation, commercial availability, lower molecular weight, and broad substrate applicability, as well as substituent compatibility of this catalysis system render oxazolidin-2-one great advantages over the Cu-catalyzed methods that have already been utilized in a number of applications.
N-hydroxyimides as efficient ligands for the copper-catalyzed N-arylation of pyrrole, imidazole, and indole
Ma, Heng-Chang,Jiang, Xuan-Zhen
, p. 8943 - 8946 (2008/03/12)
(Chemical Equation Presented) An experimentally simple, efficient, and inexpensive catalyst system was developed for the N-arylation of pyrroles, indoles, and imidazole with aryl and heteroaryl iodides, bro-mides, and chlorides by applying CuI as catalyst, N-hydroxysuccinimide (L1), N-hydroxymaleimide (L2), or N-hydroxyphthalimide (L3) as ligand, CH3ONa as base, and DMSO as solvent. A variety of functional groups are tolerated in the reaction, including those that are not compatible with Pd-catalyzed amidation methodology.
