Category: 2208-59-5

Safety of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, is researched, Molecular C12H9N3, CAS is 2208-59-5, about Microwave-assisted synthesis of aryl and heteroaryl derivatives of benzimidazole. Author is Yu, Haitao; Kawanishi, Hirohisa; Koshima, Hideko.

A series of benzimidazoles containing aryl and heteroaryl substituents were efficiently and quickly synthesized by condensation of 1,2-phenylenediamine with carboxylic acids in the presence of polyphosphoric acid under microwave irradiation For example, microwave irradiation of a mixture of 1,2-phenylenediamine, p-octylbenzoic acid, and polyphosphoric acid for 2.5 min gave 73% 2-(p-octylphenyl)-1H-benzimidazole.

Here is a brief introduction to this compound(2208-59-5)Safety of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, if you want to know about other compounds related to this compound(2208-59-5), you can read my other articles.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 2208-59-5, is researched, SMILESS is C1(C2=CC=NC=C2)=NC3=CC=CC=C3N1, Molecular C12H9N3Journal, Inorganica Chimica Acta called Unusual hexamers and infinite water chains trapped in the complexes of 2-(4-pyridyl)benzimidazole, Author is Xia, Chang-Kun; Lu, Can-Zhong; Wu, Xiao-Yuan; Chen, Li-Juan; Zhang, Quan-Zheng; Zhang, Jian-Jun; Wu, Ding-Ming, the main research direction is silver pyridylbenzimidazole complex water hexamer preparation structure; pyridylbenzimidazole terephthalate complex water trapped preparation structure; crystal structure pyridylbenzimidazole terephthalate silver complex water trapped.Reference of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole.

Unusual hexamers and H2O chains were observed in the complexes of (HPyBIm)+•(Hterephate)-•(PyBIm)·4H2O (1) and [Ag2(PyBIm)2(μ2-SO4)]·4H2O (2), resp. (PyBIm = 2-(4-pyridyl)benzimidazole). In 1, a chair-shaped hexamer (not H2O hexamer) formed by the H2O mols. and carboxylate groups as well as 1-dimensional H2O chain are being observed While in 2, a H2O hexamer-shaped as parallelogram was obtained; more interestingly, the parallelogram-shaped H2O hexamers are further aggregated into tape like infinite H2O chain via H-bonding interactions.

Here is a brief introduction to this compound(2208-59-5)Reference of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, if you want to know about other compounds related to this compound(2208-59-5), you can read my other articles.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, is researched, Molecular C12H9N3, CAS is 2208-59-5, about Dealkylation of N-pyridylethyl-2-arylbenzimidazoles by aluminum chloride.Category: indole-building-block.

Dealkylation of I (R = 2- or 4-pyridyl, R1 = Ph, 2- or 4-pyridyl), prepared by alkylation of the corresponding benzimidazole with 2- or 4-vinylpyridine, with AlCl3 in CCl4 5 h at 150° gave II (R1 as above) in 30-40% yields when R = 2-pyridyl and 85-90% yields when R = 4-pyridyl.

If you want to learn more about this compound(2-(Pyridin-4-yl)-1H-benzo[d]imidazole)Category: indole-building-block, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(2208-59-5).

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Tetrahedron Letters called Practical application of PhI(OAc)2/I2 combination to synthesize benzimidazoles from 2-aminobenzylamine through ring distortion strategy, Author is Saha, Moumita; Mukherjee, Prasun; Das, Asish R., which mentions a compound: 2208-59-5, SMILESS is C1(C2=CC=NC=C2)=NC3=CC=CC=C3N1, Molecular C12H9N3, Reference of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole.

In this present work, the combination of iodobenzenediacetate (PIDA)/iodine has been established as a promising reagent to promote the construction of 2-substituted benzimidazoles from 2-aminobenzylamine and a variety of easily available aldehydes/arylamines through a ring distortion strategy. The present protocol offers mild, metal free, robust conditions to synthesize 2-substituted benzimidazoles in good to excellent yields. In addition, the oxidation prone functional groups show tolerance during the reaction and after completion of the reaction pure products can be easily obtained applying hassle free filtration of the reaction mixture through silica gel bed.

If you want to learn more about this compound(2-(Pyridin-4-yl)-1H-benzo[d]imidazole)Reference of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(2208-59-5).

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, is researched, Molecular C12H9N3, CAS is 2208-59-5, about BF3·Et2O-promoted one-pot expeditious and convenient synthesis of 2-substituted benzimidazoles and 3,1,5-benzoxadiazepines.SDS of cas: 2208-59-5.

2-Substituted benzimidazoles, e.g., I, and 3,1,5-benzoxadiazepines, e.g., II, have been synthesized in excellent yields. The cyclodehydration of N-acyl-1,2-phenylenediamines and N,N’-diacyl-1,2-phenylenediamines, prepared in situ from the corresponding 1,2-phenylenediamines, with acid chlorides gave benzimidazoles and 3,1,5-benzoxadiazepines, resp.

Here is a brief introduction to this compound(2208-59-5)SDS of cas: 2208-59-5, if you want to know about other compounds related to this compound(2208-59-5), you can read my other articles.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles