Category: 114834-02-5

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 4-Chloro-6-(1H-imidazol-1-yl)pyrimidine, is researched, Molecular C7H5ClN4, CAS is 114834-02-5, about An electrochemical synthesis of functionalized arylpyrimidines from 4-amino-6-chloropyrimidines and aryl halides, the main research direction is aminochloropyrimidine aryl halide electrochem cross coupling nickel catalyst; biaryl heteroaryl preparation.Recommanded Product: 114834-02-5.

A range of novel 4-amino-6-arylpyrimidines was prepared under mild conditions by an electrochem. reductive cross-coupling between 4-amino-6-chloro-pyrimidines and functionalized aryl halides. The process, which employed a sacrificial iron anode in conjunction with a nickel(II) catalyst, allows the formation of coupling products in moderate to high yields.

There is still a lot of research devoted to this compound(SMILES：ClC1=NC=NC(N2C=CN=C2)=C1)Recommanded Product: 114834-02-5, and with the development of science, more effects of this compound(114834-02-5) can be discovered.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider

Synthetic Route of C7H5ClN4. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 4-Chloro-6-(1H-imidazol-1-yl)pyrimidine, is researched, Molecular C7H5ClN4, CAS is 114834-02-5, about Selective mono-amination of dichlorodiazines. Author is Sengmany, Stephane; Lebre, Julie; Le Gall, Erwan; Leonel, Eric.

3,6-Dichloropyridazine, 4,6-dichloropyrimidine, 2,4-dichloropyrimidine, and 3,5-dichloropyridazine underwent chemoselective monosubstitution reactions with amines using triethylamine as a base in ethanol at either ambient temperature or reflux to give monoamino monochloro pyridazines and pyrimidines. The methodol. is general and efficient despite noticeable differences in reactivity between diazines; while dichloropyridazine and dichloropyrazine require several hours of heating at reflux for the reaction to proceed, dichloropyrimidines reach completion within minutes at room temperature

Here is a brief introduction to this compound(114834-02-5)Synthetic Route of C7H5ClN4, if you want to know about other compounds related to this compound(114834-02-5), you can read my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider

SDS of cas: 114834-02-5. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 4-Chloro-6-(1H-imidazol-1-yl)pyrimidine, is researched, Molecular C7H5ClN4, CAS is 114834-02-5, about An electrochemical synthesis of functionalized arylpyrimidines from 4-amino-6-chloropyrimidines and aryl halides. Author is Sengmany, Stephane; Le Gall, Erwan; Leonel, Eric.

A range of novel 4-amino-6-arylpyrimidines was prepared under mild conditions by an electrochem. reductive cross-coupling between 4-amino-6-chloro-pyrimidines and functionalized aryl halides. The process, which employed a sacrificial iron anode in conjunction with a nickel(II) catalyst, allows the formation of coupling products in moderate to high yields.

In some applications, this compound(114834-02-5)SDS of cas: 114834-02-5 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider